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Items: 1 to 20 of 856

1.

rs1489742504 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    17:59049246 (GRCh38)
    17:57126607 (GRCh37)
    Canonical SPDI:
    NC_000017.11:59049245:T:C
    Gene:
    TRIM37 (Varview)
    Functional Consequence:
    non_coding_transcript_variant,coding_sequence_variant,missense_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0./0 (ALFA)
    C=0.000004/1 (GnomAD_exomes)
    C=0.000015/4 (TOPMED)
    C=0.000029/4 (GnomAD)
    HGVS:
    NC_000017.11:g.59049246T>C, NC_000017.10:g.57126607T>C, NG_009298.1:g.62660A>G, NM_015294.6:c.1462A>G, NM_015294.5:c.1462A>G, NM_015294.4:c.1462A>G, NM_015294.3:c.1462A>G, NM_001005207.5:c.1462A>G, NM_001005207.4:c.1462A>G, NM_001005207.3:c.1462A>G, NM_001005207.2:c.1462A>G, NM_001320990.3:c.1096A>G, NM_001320990.2:c.1096A>G, NM_001320990.1:c.1096A>G, NM_001320987.3:c.1360A>G, NM_001320987.2:c.1360A>G, NM_001320987.1:c.1360A>G, NM_001320988.3:c.1462A>G, NM_001320988.2:c.1462A>G, NM_001320988.1:c.1462A>G, NM_001320989.3:c.1462A>G, NM_001320989.2:c.1462A>G, NM_001320989.1:c.1462A>G, NR_148346.2:n.1881A>G, NR_148346.1:n.1965A>G, NM_001353084.2:c.1462A>G, NM_001353084.1:c.1462A>G, NM_001353083.2:c.727A>G, NM_001353083.1:c.727A>G, NM_001353086.2:c.1411A>G, NM_001353086.1:c.1411A>G, NR_148347.2:n.1779A>G, NR_148347.1:n.1863A>G, NM_001353082.2:c.1360A>G, NM_001353082.1:c.1360A>G, NM_001353085.2:c.1000A>G, NM_001353085.1:c.1000A>G, XM_011524832.3:c.1462A>G, XM_011524832.2:c.1462A>G, XM_011524832.1:c.1462A>G, XM_017024663.3:c.1462A>G, XM_017024663.2:c.1462A>G, XM_017024663.1:c.1462A>G, XM_017024669.3:c.1309A>G, XM_017024669.2:c.1309A>G, XM_017024669.1:c.1309A>G, XM_017024670.3:c.1360A>G, XM_017024670.2:c.1360A>G, XM_017024670.1:c.1360A>G, XM_017024673.3:c.727A>G, XM_017024673.2:c.727A>G, XM_017024673.1:c.727A>G, XM_017024662.2:c.1462A>G, XM_017024662.1:c.1462A>G, XM_011524831.2:c.1462A>G, XM_011524831.1:c.1462A>G, XM_017024665.2:c.1360A>G, XM_017024665.1:c.1360A>G, XM_011524836.2:c.1462A>G, XM_011524836.1:c.1462A>G, XM_005257385.2:c.1462A>G, XM_005257385.1:c.1462A>G, XM_017024667.2:c.1411A>G, XM_017024667.1:c.1411A>G, XM_011524833.2:c.1411A>G, XM_011524833.1:c.1411A>G, XM_011524834.2:c.1360A>G, XM_011524834.1:c.1360A>G, XM_047436107.1:c.1360A>G, XM_047436110.1:c.1360A>G, XM_047436111.1:c.1462A>G, XM_047436106.1:c.1411A>G, XM_047436109.1:c.1462A>G, XM_047436119.1:c.1411A>G, XM_047436120.1:c.1360A>G, XM_047436124.1:c.1309A>G, XM_047436125.1:c.1309A>G, XM_047436126.1:c.1360A>G, XM_047436108.1:c.1411A>G, XM_047436113.1:c.1360A>G, XM_047436115.1:c.1462A>G, XM_047436114.1:c.1360A>G, XM_047436116.1:c.1462A>G, XM_047436117.1:c.1411A>G, XM_047436121.1:c.1360A>G, XM_047436122.1:c.1360A>G, XM_047436123.1:c.1462A>G, XM_047436112.1:c.1309A>G, XM_047436118.1:c.1462A>G, NP_056109.1:p.Thr488Ala, NP_001005207.1:p.Thr488Ala, NP_001307919.1:p.Thr366Ala, NP_001307916.1:p.Thr454Ala, NP_001307917.1:p.Thr488Ala, NP_001307918.1:p.Thr488Ala, NP_001340013.1:p.Thr488Ala, NP_001340012.1:p.Thr243Ala, NP_001340015.1:p.Thr471Ala, NP_001340011.1:p.Thr454Ala, NP_001340014.1:p.Thr334Ala, XP_011523134.1:p.Thr488Ala, XP_016880152.1:p.Thr488Ala, XP_016880158.1:p.Thr437Ala, XP_016880159.1:p.Thr454Ala, XP_016880162.1:p.Thr243Ala, XP_016880151.1:p.Thr488Ala, XP_011523133.1:p.Thr488Ala, XP_016880154.1:p.Thr454Ala, XP_011523138.1:p.Thr488Ala, XP_005257442.1:p.Thr488Ala, XP_016880156.1:p.Thr471Ala, XP_011523135.1:p.Thr471Ala, XP_011523136.1:p.Thr454Ala, XP_047292063.1:p.Thr454Ala, XP_047292066.1:p.Thr454Ala, XP_047292067.1:p.Thr488Ala, XP_047292062.1:p.Thr471Ala, XP_047292065.1:p.Thr488Ala, XP_047292075.1:p.Thr471Ala, XP_047292076.1:p.Thr454Ala, XP_047292080.1:p.Thr437Ala, XP_047292081.1:p.Thr437Ala, XP_047292082.1:p.Thr454Ala, XP_047292064.1:p.Thr471Ala, XP_047292069.1:p.Thr454Ala, XP_047292071.1:p.Thr488Ala, XP_047292070.1:p.Thr454Ala, XP_047292072.1:p.Thr488Ala, XP_047292073.1:p.Thr471Ala, XP_047292077.1:p.Thr454Ala, XP_047292078.1:p.Thr454Ala, XP_047292079.1:p.Thr488Ala, XP_047292068.1:p.Thr437Ala, XP_047292074.1:p.Thr488Ala

    2.

    rs1487459885 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G [Show Flanks]
      Chromosome:
      17:59106448 (GRCh38)
      17:57183809 (GRCh37)
      Canonical SPDI:
      NC_000017.11:59106447:C:G
      Gene:
      TRIM37 (Varview), LOC124904039 (Varview)
      Functional Consequence:
      coding_sequence_variant,2KB_upstream_variant,non_coding_transcript_variant,5_prime_UTR_variant,missense_variant,upstream_transcript_variant,genic_upstream_transcript_variant
      Validated:
      by frequency
      MAF:
      G=0.000004/1 (GnomAD_exomes)
      HGVS:
      NC_000017.11:g.59106448C>G, NC_000017.10:g.57183809C>G, NG_009298.1:g.5458G>C, NM_015294.6:c.14G>C, NM_015294.5:c.14G>C, NM_015294.4:c.14G>C, NM_015294.3:c.14G>C, NM_001005207.5:c.14G>C, NM_001005207.4:c.14G>C, NM_001005207.3:c.14G>C, NM_001005207.2:c.14G>C, NM_001320990.3:c.-429G>C, NM_001320990.2:c.-429G>C, NM_001320990.1:c.-429G>C, NM_001320987.3:c.14G>C, NM_001320987.2:c.14G>C, NM_001320987.1:c.14G>C, NM_001320988.3:c.14G>C, NM_001320988.2:c.14G>C, NM_001320988.1:c.14G>C, NM_001320989.3:c.14G>C, NM_001320989.2:c.14G>C, NM_001320989.1:c.14G>C, NR_148346.2:n.433G>C, NR_148346.1:n.517G>C, NM_001353084.2:c.14G>C, NM_001353084.1:c.14G>C, NM_001353083.2:c.-739G>C, NM_001353083.1:c.-739G>C, NM_001353086.2:c.14G>C, NM_001353086.1:c.14G>C, NR_148347.2:n.433G>C, NR_148347.1:n.517G>C, NM_001353082.2:c.14G>C, NM_001353082.1:c.14G>C, NM_001353085.2:c.-259G>C, NM_001353085.1:c.-259G>C, XM_011524832.3:c.14G>C, XM_011524832.2:c.14G>C, XM_011524832.1:c.14G>C, XM_017024663.3:c.14G>C, XM_017024663.2:c.14G>C, XM_017024663.1:c.14G>C, XM_017024669.3:c.14G>C, XM_017024669.2:c.14G>C, XM_017024669.1:c.14G>C, XM_017024670.3:c.14G>C, XM_017024670.2:c.14G>C, XM_017024670.1:c.14G>C, XM_017024662.2:c.14G>C, XM_017024662.1:c.14G>C, XM_011524831.2:c.14G>C, XM_011524831.1:c.14G>C, XM_017024665.2:c.14G>C, XM_017024665.1:c.14G>C, XM_011524836.2:c.14G>C, XM_011524836.1:c.14G>C, XM_005257385.2:c.14G>C, XM_005257385.1:c.14G>C, XM_017024667.2:c.14G>C, XM_017024667.1:c.14G>C, XM_011524833.2:c.14G>C, XM_011524833.1:c.14G>C, XM_011524834.2:c.14G>C, XM_011524834.1:c.14G>C, XM_047436107.1:c.14G>C, XM_047436110.1:c.14G>C, XM_047436111.1:c.14G>C, XM_047436106.1:c.14G>C, XM_047436109.1:c.14G>C, XM_047436119.1:c.14G>C, XM_047436120.1:c.14G>C, XM_047436124.1:c.14G>C, XM_047436125.1:c.14G>C, XM_047436126.1:c.14G>C, XM_047436108.1:c.14G>C, XM_047436113.1:c.14G>C, XM_047436115.1:c.14G>C, XM_047436114.1:c.14G>C, XM_047436116.1:c.14G>C, XM_047436117.1:c.14G>C, XM_047436121.1:c.14G>C, XM_047436122.1:c.14G>C, XM_047436123.1:c.14G>C, XM_047436112.1:c.14G>C, XM_047436118.1:c.14G>C, NP_056109.1:p.Ser5Thr, NP_001005207.1:p.Ser5Thr, NP_001307916.1:p.Ser5Thr, NP_001307917.1:p.Ser5Thr, NP_001307918.1:p.Ser5Thr, NP_001340013.1:p.Ser5Thr, NP_001340015.1:p.Ser5Thr, NP_001340011.1:p.Ser5Thr, XP_011523134.1:p.Ser5Thr, XP_016880152.1:p.Ser5Thr, XP_016880158.1:p.Ser5Thr, XP_016880159.1:p.Ser5Thr, XP_016880151.1:p.Ser5Thr, XP_011523133.1:p.Ser5Thr, XP_016880154.1:p.Ser5Thr, XP_011523138.1:p.Ser5Thr, XP_005257442.1:p.Ser5Thr, XP_016880156.1:p.Ser5Thr, XP_011523135.1:p.Ser5Thr, XP_011523136.1:p.Ser5Thr, XP_047292063.1:p.Ser5Thr, XP_047292066.1:p.Ser5Thr, XP_047292067.1:p.Ser5Thr, XP_047292062.1:p.Ser5Thr, XP_047292065.1:p.Ser5Thr, XP_047292075.1:p.Ser5Thr, XP_047292076.1:p.Ser5Thr, XP_047292080.1:p.Ser5Thr, XP_047292081.1:p.Ser5Thr, XP_047292082.1:p.Ser5Thr, XP_047292064.1:p.Ser5Thr, XP_047292069.1:p.Ser5Thr, XP_047292071.1:p.Ser5Thr, XP_047292070.1:p.Ser5Thr, XP_047292072.1:p.Ser5Thr, XP_047292073.1:p.Ser5Thr, XP_047292077.1:p.Ser5Thr, XP_047292078.1:p.Ser5Thr, XP_047292079.1:p.Ser5Thr, XP_047292068.1:p.Ser5Thr, XP_047292074.1:p.Ser5Thr

      3.

      rs1484746557 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C [Show Flanks]
        Chromosome:
        17:59015715 (GRCh38)
        17:57093076 (GRCh37)
        Canonical SPDI:
        NC_000017.11:59015714:T:C
        Gene:
        TRIM37 (Varview)
        Functional Consequence:
        non_coding_transcript_variant,coding_sequence_variant,missense_variant
        Validated:
        by frequency,by alfa
        MAF:
        C=0.000111/1 (ALFA)
        C=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000017.11:g.59015715T>C, NC_000017.10:g.57093076T>C, NG_009298.1:g.96191A>G, NM_015294.6:c.2471A>G, NM_015294.5:c.2471A>G, NM_015294.4:c.2471A>G, NM_015294.3:c.2471A>G, NM_001005207.5:c.2471A>G, NM_001005207.4:c.2471A>G, NM_001005207.3:c.2471A>G, NM_001005207.2:c.2471A>G, NM_001320990.3:c.2105A>G, NM_001320990.2:c.2105A>G, NM_001320990.1:c.2105A>G, NM_001320987.3:c.2369A>G, NM_001320987.2:c.2369A>G, NM_001320987.1:c.2369A>G, NM_001320988.3:c.2471A>G, NM_001320988.2:c.2471A>G, NM_001320988.1:c.2471A>G, NM_001320989.3:c.2471A>G, NM_001320989.2:c.2471A>G, NM_001320989.1:c.2471A>G, NR_148346.2:n.2890A>G, NR_148346.1:n.2974A>G, NM_001353084.2:c.2471A>G, NM_001353084.1:c.2471A>G, NM_001353083.2:c.1736A>G, NM_001353083.1:c.1736A>G, NM_001353086.2:c.2420A>G, NM_001353086.1:c.2420A>G, NR_148347.2:n.2788A>G, NR_148347.1:n.2872A>G, NM_001353082.2:c.2369A>G, NM_001353082.1:c.2369A>G, NM_001353085.2:c.2009A>G, NM_001353085.1:c.2009A>G, XM_011524832.3:c.2471A>G, XM_011524832.2:c.2471A>G, XM_011524832.1:c.2471A>G, XM_017024663.3:c.2471A>G, XM_017024663.2:c.2471A>G, XM_017024663.1:c.2471A>G, XM_017024669.3:c.2318A>G, XM_017024669.2:c.2318A>G, XM_017024669.1:c.2318A>G, XM_017024670.3:c.2369A>G, XM_017024670.2:c.2369A>G, XM_017024670.1:c.2369A>G, XM_017024673.3:c.1736A>G, XM_017024673.2:c.1736A>G, XM_017024673.1:c.1736A>G, XM_017024662.2:c.2471A>G, XM_017024662.1:c.2471A>G, XM_011524831.2:c.2471A>G, XM_011524831.1:c.2471A>G, XM_017024665.2:c.2369A>G, XM_017024665.1:c.2369A>G, XM_011524836.2:c.2471A>G, XM_011524836.1:c.2471A>G, XM_005257385.2:c.2471A>G, XM_005257385.1:c.2471A>G, XM_017024667.2:c.2420A>G, XM_017024667.1:c.2420A>G, XM_011524833.2:c.2420A>G, XM_011524833.1:c.2420A>G, XM_011524834.2:c.2369A>G, XM_011524834.1:c.2369A>G, XM_047436107.1:c.2369A>G, XM_047436110.1:c.2369A>G, XM_047436111.1:c.2471A>G, XM_047436106.1:c.2420A>G, XM_047436109.1:c.2342A>G, XM_047436119.1:c.2291A>G, XM_047436120.1:c.2240A>G, XM_047436124.1:c.2318A>G, XM_047436125.1:c.2189A>G, XM_047436126.1:c.2240A>G, XM_047436108.1:c.2420A>G, XM_047436113.1:c.2369A>G, XM_047436115.1:c.2342A>G, XM_047436114.1:c.2369A>G, XM_047436116.1:c.2342A>G, XM_047436117.1:c.2420A>G, XM_047436121.1:c.2369A>G, XM_047436122.1:c.2240A>G, XM_047436123.1:c.2342A>G, XM_047436112.1:c.2318A>G, XM_047436118.1:c.2342A>G, NP_056109.1:p.Lys824Arg, NP_001005207.1:p.Lys824Arg, NP_001307919.1:p.Lys702Arg, NP_001307916.1:p.Lys790Arg, NP_001307917.1:p.Lys824Arg, NP_001307918.1:p.Lys824Arg, NP_001340013.1:p.Lys824Arg, NP_001340012.1:p.Lys579Arg, NP_001340015.1:p.Lys807Arg, NP_001340011.1:p.Lys790Arg, NP_001340014.1:p.Lys670Arg, XP_011523134.1:p.Lys824Arg, XP_016880152.1:p.Lys824Arg, XP_016880158.1:p.Lys773Arg, XP_016880159.1:p.Lys790Arg, XP_016880162.1:p.Lys579Arg, XP_016880151.1:p.Lys824Arg, XP_011523133.1:p.Lys824Arg, XP_016880154.1:p.Lys790Arg, XP_011523138.1:p.Lys824Arg, XP_005257442.1:p.Lys824Arg, XP_016880156.1:p.Lys807Arg, XP_011523135.1:p.Lys807Arg, XP_011523136.1:p.Lys790Arg, XP_047292063.1:p.Lys790Arg, XP_047292066.1:p.Lys790Arg, XP_047292067.1:p.Lys824Arg, XP_047292062.1:p.Lys807Arg, XP_047292065.1:p.Lys781Arg, XP_047292075.1:p.Lys764Arg, XP_047292076.1:p.Lys747Arg, XP_047292080.1:p.Lys773Arg, XP_047292081.1:p.Lys730Arg, XP_047292082.1:p.Lys747Arg, XP_047292064.1:p.Lys807Arg, XP_047292069.1:p.Lys790Arg, XP_047292071.1:p.Lys781Arg, XP_047292070.1:p.Lys790Arg, XP_047292072.1:p.Lys781Arg, XP_047292073.1:p.Lys807Arg, XP_047292077.1:p.Lys790Arg, XP_047292078.1:p.Lys747Arg, XP_047292079.1:p.Lys781Arg, XP_047292068.1:p.Lys773Arg, XP_047292074.1:p.Lys781Arg

        4.

        rs1484570929 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          A>- [Show Flanks]
          Chromosome:
          17:59062572 (GRCh38)
          17:57139933 (GRCh37)
          Canonical SPDI:
          NC_000017.11:59062571:AAA:AA
          Gene:
          TRIM37 (Varview)
          Functional Consequence:
          non_coding_transcript_variant,coding_sequence_variant,frameshift_variant
          Validated:
          by frequency,by alfa
          MAF:
          AA=0./0 (ALFA)
          -=0.000008/2 (TOPMED)
          HGVS:
          NC_000017.11:g.59062574del, NC_000017.10:g.57139935del, NG_009298.1:g.49334del, NM_015294.6:c.937del, NM_015294.5:c.937del, NM_015294.4:c.937del, NM_015294.3:c.937del, NM_001005207.5:c.937del, NM_001005207.4:c.937del, NM_001005207.3:c.937del, NM_001005207.2:c.937del, NM_001320990.3:c.571del, NM_001320990.2:c.571del, NM_001320990.1:c.571del, NM_001320987.3:c.835del, NM_001320987.2:c.835del, NM_001320987.1:c.835del, NM_001320988.3:c.937del, NM_001320988.2:c.937del, NM_001320988.1:c.937del, NM_001320989.3:c.937del, NM_001320989.2:c.937del, NM_001320989.1:c.937del, NR_148346.2:n.1356del, NR_148346.1:n.1440del, NM_001353084.2:c.937del, NM_001353084.1:c.937del, NM_001353083.2:c.202del, NM_001353083.1:c.202del, NM_001353086.2:c.886del, NM_001353086.1:c.886del, NR_148347.2:n.1254del, NR_148347.1:n.1338del, NM_001353082.2:c.835del, NM_001353082.1:c.835del, NM_001353085.2:c.475del, NM_001353085.1:c.475del, XM_011524832.3:c.937del, XM_011524832.2:c.937del, XM_011524832.1:c.937del, XM_017024663.3:c.937del, XM_017024663.2:c.937del, XM_017024663.1:c.937del, XM_017024669.3:c.784del, XM_017024669.2:c.784del, XM_017024669.1:c.784del, XM_017024670.3:c.835del, XM_017024670.2:c.835del, XM_017024670.1:c.835del, XM_017024673.3:c.202del, XM_017024673.2:c.202del, XM_017024673.1:c.202del, XM_017024662.2:c.937del, XM_017024662.1:c.937del, XM_011524831.2:c.937del, XM_011524831.1:c.937del, XM_017024665.2:c.835del, XM_017024665.1:c.835del, XM_011524836.2:c.937del, XM_011524836.1:c.937del, XM_005257385.2:c.937del, XM_005257385.1:c.937del, XM_017024667.2:c.886del, XM_017024667.1:c.886del, XM_011524833.2:c.886del, XM_011524833.1:c.886del, XM_011524834.2:c.835del, XM_011524834.1:c.835del, XM_047436107.1:c.835del, XM_047436110.1:c.835del, XM_047436111.1:c.937del, XM_047436106.1:c.886del, XM_047436109.1:c.937del, XM_047436119.1:c.886del, XM_047436120.1:c.835del, XM_047436124.1:c.784del, XM_047436125.1:c.784del, XM_047436126.1:c.835del, XM_047436108.1:c.886del, XM_047436113.1:c.835del, XM_047436115.1:c.937del, XM_047436114.1:c.835del, XM_047436116.1:c.937del, XM_047436117.1:c.886del, XM_047436121.1:c.835del, XM_047436122.1:c.835del, XM_047436123.1:c.937del, XM_047436112.1:c.784del, XM_047436118.1:c.937del, NP_056109.1:p.Tyr313fs, NP_001005207.1:p.Tyr313fs, NP_001307919.1:p.Tyr191fs, NP_001307916.1:p.Tyr279fs, NP_001307917.1:p.Tyr313fs, NP_001307918.1:p.Tyr313fs, NP_001340013.1:p.Tyr313fs, NP_001340012.1:p.Tyr68fs, NP_001340015.1:p.Tyr296fs, NP_001340011.1:p.Tyr279fs, NP_001340014.1:p.Tyr159fs, XP_011523134.1:p.Tyr313fs, XP_016880152.1:p.Tyr313fs, XP_016880158.1:p.Tyr262fs, XP_016880159.1:p.Tyr279fs, XP_016880162.1:p.Tyr68fs, XP_016880151.1:p.Tyr313fs, XP_011523133.1:p.Tyr313fs, XP_016880154.1:p.Tyr279fs, XP_011523138.1:p.Tyr313fs, XP_005257442.1:p.Tyr313fs, XP_016880156.1:p.Tyr296fs, XP_011523135.1:p.Tyr296fs, XP_011523136.1:p.Tyr279fs, XP_047292063.1:p.Tyr279fs, XP_047292066.1:p.Tyr279fs, XP_047292067.1:p.Tyr313fs, XP_047292062.1:p.Tyr296fs, XP_047292065.1:p.Tyr313fs, XP_047292075.1:p.Tyr296fs, XP_047292076.1:p.Tyr279fs, XP_047292080.1:p.Tyr262fs, XP_047292081.1:p.Tyr262fs, XP_047292082.1:p.Tyr279fs, XP_047292064.1:p.Tyr296fs, XP_047292069.1:p.Tyr279fs, XP_047292071.1:p.Tyr313fs, XP_047292070.1:p.Tyr279fs, XP_047292072.1:p.Tyr313fs, XP_047292073.1:p.Tyr296fs, XP_047292077.1:p.Tyr279fs, XP_047292078.1:p.Tyr279fs, XP_047292079.1:p.Tyr313fs, XP_047292068.1:p.Tyr262fs, XP_047292074.1:p.Tyr313fs

          5.

          rs1483701810 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>C [Show Flanks]
            Chromosome:
            17:59049323 (GRCh38)
            17:57126684 (GRCh37)
            Canonical SPDI:
            NC_000017.11:59049322:G:C
            Gene:
            TRIM37 (Varview)
            Functional Consequence:
            non_coding_transcript_variant,coding_sequence_variant,missense_variant
            Validated:
            by frequency,by cluster
            MAF:
            C=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000017.11:g.59049323G>C, NC_000017.10:g.57126684G>C, NG_009298.1:g.62583C>G, NM_015294.6:c.1385C>G, NM_015294.5:c.1385C>G, NM_015294.4:c.1385C>G, NM_015294.3:c.1385C>G, NM_001005207.5:c.1385C>G, NM_001005207.4:c.1385C>G, NM_001005207.3:c.1385C>G, NM_001005207.2:c.1385C>G, NM_001320990.3:c.1019C>G, NM_001320990.2:c.1019C>G, NM_001320990.1:c.1019C>G, NM_001320987.3:c.1283C>G, NM_001320987.2:c.1283C>G, NM_001320987.1:c.1283C>G, NM_001320988.3:c.1385C>G, NM_001320988.2:c.1385C>G, NM_001320988.1:c.1385C>G, NM_001320989.3:c.1385C>G, NM_001320989.2:c.1385C>G, NM_001320989.1:c.1385C>G, NR_148346.2:n.1804C>G, NR_148346.1:n.1888C>G, NM_001353084.2:c.1385C>G, NM_001353084.1:c.1385C>G, NM_001353083.2:c.650C>G, NM_001353083.1:c.650C>G, NM_001353086.2:c.1334C>G, NM_001353086.1:c.1334C>G, NR_148347.2:n.1702C>G, NR_148347.1:n.1786C>G, NM_001353082.2:c.1283C>G, NM_001353082.1:c.1283C>G, NM_001353085.2:c.923C>G, NM_001353085.1:c.923C>G, XM_011524832.3:c.1385C>G, XM_011524832.2:c.1385C>G, XM_011524832.1:c.1385C>G, XM_017024663.3:c.1385C>G, XM_017024663.2:c.1385C>G, XM_017024663.1:c.1385C>G, XM_017024669.3:c.1232C>G, XM_017024669.2:c.1232C>G, XM_017024669.1:c.1232C>G, XM_017024670.3:c.1283C>G, XM_017024670.2:c.1283C>G, XM_017024670.1:c.1283C>G, XM_017024673.3:c.650C>G, XM_017024673.2:c.650C>G, XM_017024673.1:c.650C>G, XM_017024662.2:c.1385C>G, XM_017024662.1:c.1385C>G, XM_011524831.2:c.1385C>G, XM_011524831.1:c.1385C>G, XM_017024665.2:c.1283C>G, XM_017024665.1:c.1283C>G, XM_011524836.2:c.1385C>G, XM_011524836.1:c.1385C>G, XM_005257385.2:c.1385C>G, XM_005257385.1:c.1385C>G, XM_017024667.2:c.1334C>G, XM_017024667.1:c.1334C>G, XM_011524833.2:c.1334C>G, XM_011524833.1:c.1334C>G, XM_011524834.2:c.1283C>G, XM_011524834.1:c.1283C>G, XM_047436107.1:c.1283C>G, XM_047436110.1:c.1283C>G, XM_047436111.1:c.1385C>G, XM_047436106.1:c.1334C>G, XM_047436109.1:c.1385C>G, XM_047436119.1:c.1334C>G, XM_047436120.1:c.1283C>G, XM_047436124.1:c.1232C>G, XM_047436125.1:c.1232C>G, XM_047436126.1:c.1283C>G, XM_047436108.1:c.1334C>G, XM_047436113.1:c.1283C>G, XM_047436115.1:c.1385C>G, XM_047436114.1:c.1283C>G, XM_047436116.1:c.1385C>G, XM_047436117.1:c.1334C>G, XM_047436121.1:c.1283C>G, XM_047436122.1:c.1283C>G, XM_047436123.1:c.1385C>G, XM_047436112.1:c.1232C>G, XM_047436118.1:c.1385C>G, NP_056109.1:p.Pro462Arg, NP_001005207.1:p.Pro462Arg, NP_001307919.1:p.Pro340Arg, NP_001307916.1:p.Pro428Arg, NP_001307917.1:p.Pro462Arg, NP_001307918.1:p.Pro462Arg, NP_001340013.1:p.Pro462Arg, NP_001340012.1:p.Pro217Arg, NP_001340015.1:p.Pro445Arg, NP_001340011.1:p.Pro428Arg, NP_001340014.1:p.Pro308Arg, XP_011523134.1:p.Pro462Arg, XP_016880152.1:p.Pro462Arg, XP_016880158.1:p.Pro411Arg, XP_016880159.1:p.Pro428Arg, XP_016880162.1:p.Pro217Arg, XP_016880151.1:p.Pro462Arg, XP_011523133.1:p.Pro462Arg, XP_016880154.1:p.Pro428Arg, XP_011523138.1:p.Pro462Arg, XP_005257442.1:p.Pro462Arg, XP_016880156.1:p.Pro445Arg, XP_011523135.1:p.Pro445Arg, XP_011523136.1:p.Pro428Arg, XP_047292063.1:p.Pro428Arg, XP_047292066.1:p.Pro428Arg, XP_047292067.1:p.Pro462Arg, XP_047292062.1:p.Pro445Arg, XP_047292065.1:p.Pro462Arg, XP_047292075.1:p.Pro445Arg, XP_047292076.1:p.Pro428Arg, XP_047292080.1:p.Pro411Arg, XP_047292081.1:p.Pro411Arg, XP_047292082.1:p.Pro428Arg, XP_047292064.1:p.Pro445Arg, XP_047292069.1:p.Pro428Arg, XP_047292071.1:p.Pro462Arg, XP_047292070.1:p.Pro428Arg, XP_047292072.1:p.Pro462Arg, XP_047292073.1:p.Pro445Arg, XP_047292077.1:p.Pro428Arg, XP_047292078.1:p.Pro428Arg, XP_047292079.1:p.Pro462Arg, XP_047292068.1:p.Pro411Arg, XP_047292074.1:p.Pro462Arg

            6.

            rs1482895654 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              T>C [Show Flanks]
              Chromosome:
              17:59015632 (GRCh38)
              17:57092993 (GRCh37)
              Canonical SPDI:
              NC_000017.11:59015631:T:C
              Gene:
              TRIM37 (Varview)
              Functional Consequence:
              non_coding_transcript_variant,coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0./0 (ALFA)
              C=0.000004/1 (GnomAD_exomes)
              C=0.000004/1 (TOPMED)
              HGVS:
              NC_000017.11:g.59015632T>C, NC_000017.10:g.57092993T>C, NG_009298.1:g.96274A>G, NM_015294.6:c.2554A>G, NM_015294.5:c.2554A>G, NM_015294.4:c.2554A>G, NM_015294.3:c.2554A>G, NM_001005207.5:c.2554A>G, NM_001005207.4:c.2554A>G, NM_001005207.3:c.2554A>G, NM_001005207.2:c.2554A>G, NM_001320990.3:c.2188A>G, NM_001320990.2:c.2188A>G, NM_001320990.1:c.2188A>G, NM_001320987.3:c.2452A>G, NM_001320987.2:c.2452A>G, NM_001320987.1:c.2452A>G, NM_001320988.3:c.2554A>G, NM_001320988.2:c.2554A>G, NM_001320988.1:c.2554A>G, NM_001320989.3:c.2554A>G, NM_001320989.2:c.2554A>G, NM_001320989.1:c.2554A>G, NR_148346.2:n.2973A>G, NR_148346.1:n.3057A>G, NM_001353084.2:c.2554A>G, NM_001353084.1:c.2554A>G, NM_001353083.2:c.1819A>G, NM_001353083.1:c.1819A>G, NM_001353086.2:c.2503A>G, NM_001353086.1:c.2503A>G, NR_148347.2:n.2871A>G, NR_148347.1:n.2955A>G, NM_001353082.2:c.2452A>G, NM_001353082.1:c.2452A>G, NM_001353085.2:c.2092A>G, NM_001353085.1:c.2092A>G, XM_011524832.3:c.2554A>G, XM_011524832.2:c.2554A>G, XM_011524832.1:c.2554A>G, XM_017024663.3:c.2554A>G, XM_017024663.2:c.2554A>G, XM_017024663.1:c.2554A>G, XM_017024669.3:c.2401A>G, XM_017024669.2:c.2401A>G, XM_017024669.1:c.2401A>G, XM_017024670.3:c.2452A>G, XM_017024670.2:c.2452A>G, XM_017024670.1:c.2452A>G, XM_017024673.3:c.1819A>G, XM_017024673.2:c.1819A>G, XM_017024673.1:c.1819A>G, XM_017024662.2:c.2554A>G, XM_017024662.1:c.2554A>G, XM_011524831.2:c.2554A>G, XM_011524831.1:c.2554A>G, XM_017024665.2:c.2452A>G, XM_017024665.1:c.2452A>G, XM_011524836.2:c.2554A>G, XM_011524836.1:c.2554A>G, XM_005257385.2:c.2554A>G, XM_005257385.1:c.2554A>G, XM_017024667.2:c.2503A>G, XM_017024667.1:c.2503A>G, XM_011524833.2:c.2503A>G, XM_011524833.1:c.2503A>G, XM_011524834.2:c.2452A>G, XM_011524834.1:c.2452A>G, XM_047436107.1:c.2452A>G, XM_047436110.1:c.2452A>G, XM_047436111.1:c.2554A>G, XM_047436106.1:c.2503A>G, XM_047436109.1:c.2425A>G, XM_047436119.1:c.2374A>G, XM_047436120.1:c.2323A>G, XM_047436124.1:c.2401A>G, XM_047436125.1:c.2272A>G, XM_047436126.1:c.2323A>G, XM_047436108.1:c.2503A>G, XM_047436113.1:c.2452A>G, XM_047436115.1:c.2425A>G, XM_047436114.1:c.2452A>G, XM_047436116.1:c.2425A>G, XM_047436117.1:c.2503A>G, XM_047436121.1:c.2452A>G, XM_047436122.1:c.2323A>G, XM_047436123.1:c.2425A>G, XM_047436112.1:c.2401A>G, XM_047436118.1:c.2425A>G, NP_056109.1:p.Arg852Gly, NP_001005207.1:p.Arg852Gly, NP_001307919.1:p.Arg730Gly, NP_001307916.1:p.Arg818Gly, NP_001307917.1:p.Arg852Gly, NP_001307918.1:p.Arg852Gly, NP_001340013.1:p.Arg852Gly, NP_001340012.1:p.Arg607Gly, NP_001340015.1:p.Arg835Gly, NP_001340011.1:p.Arg818Gly, NP_001340014.1:p.Arg698Gly, XP_011523134.1:p.Arg852Gly, XP_016880152.1:p.Arg852Gly, XP_016880158.1:p.Arg801Gly, XP_016880159.1:p.Arg818Gly, XP_016880162.1:p.Arg607Gly, XP_016880151.1:p.Arg852Gly, XP_011523133.1:p.Arg852Gly, XP_016880154.1:p.Arg818Gly, XP_011523138.1:p.Arg852Gly, XP_005257442.1:p.Arg852Gly, XP_016880156.1:p.Arg835Gly, XP_011523135.1:p.Arg835Gly, XP_011523136.1:p.Arg818Gly, XP_047292063.1:p.Arg818Gly, XP_047292066.1:p.Arg818Gly, XP_047292067.1:p.Arg852Gly, XP_047292062.1:p.Arg835Gly, XP_047292065.1:p.Arg809Gly, XP_047292075.1:p.Arg792Gly, XP_047292076.1:p.Arg775Gly, XP_047292080.1:p.Arg801Gly, XP_047292081.1:p.Arg758Gly, XP_047292082.1:p.Arg775Gly, XP_047292064.1:p.Arg835Gly, XP_047292069.1:p.Arg818Gly, XP_047292071.1:p.Arg809Gly, XP_047292070.1:p.Arg818Gly, XP_047292072.1:p.Arg809Gly, XP_047292073.1:p.Arg835Gly, XP_047292077.1:p.Arg818Gly, XP_047292078.1:p.Arg775Gly, XP_047292079.1:p.Arg809Gly, XP_047292068.1:p.Arg801Gly, XP_047292074.1:p.Arg809Gly

              7.

              rs1480995534 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                T>C [Show Flanks]
                Chromosome:
                17:59088378 (GRCh38)
                17:57165739 (GRCh37)
                Canonical SPDI:
                NC_000017.11:59088377:T:C
                Gene:
                TRIM37 (Varview)
                Functional Consequence:
                coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant,missense_variant,genic_upstream_transcript_variant
                Validated:
                by frequency
                MAF:
                C=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000017.11:g.59088378T>C, NC_000017.10:g.57165739T>C, NG_009298.1:g.23528A>G, NM_015294.6:c.194A>G, NM_015294.5:c.194A>G, NM_015294.4:c.194A>G, NM_015294.3:c.194A>G, NM_001005207.5:c.194A>G, NM_001005207.4:c.194A>G, NM_001005207.3:c.194A>G, NM_001005207.2:c.194A>G, NM_001320990.3:c.-173A>G, NM_001320990.2:c.-173A>G, NM_001320990.1:c.-173A>G, NM_001320987.3:c.92A>G, NM_001320987.2:c.92A>G, NM_001320987.1:c.92A>G, NM_001320988.3:c.194A>G, NM_001320988.2:c.194A>G, NM_001320988.1:c.194A>G, NM_001320989.3:c.194A>G, NM_001320989.2:c.194A>G, NM_001320989.1:c.194A>G, NR_148346.2:n.613A>G, NR_148346.1:n.697A>G, NM_001353084.2:c.194A>G, NM_001353084.1:c.194A>G, NM_001353083.2:c.-559A>G, NM_001353083.1:c.-559A>G, NM_001353086.2:c.194A>G, NM_001353086.1:c.194A>G, NR_148347.2:n.511A>G, NR_148347.1:n.595A>G, NM_001353082.2:c.92A>G, NM_001353082.1:c.92A>G, NM_001353085.2:c.-181A>G, NM_001353085.1:c.-181A>G, XM_011524832.3:c.194A>G, XM_011524832.2:c.194A>G, XM_011524832.1:c.194A>G, XM_017024663.3:c.194A>G, XM_017024663.2:c.194A>G, XM_017024663.1:c.194A>G, XM_017024669.3:c.92A>G, XM_017024669.2:c.92A>G, XM_017024669.1:c.92A>G, XM_017024670.3:c.92A>G, XM_017024670.2:c.92A>G, XM_017024670.1:c.92A>G, XM_017024662.2:c.194A>G, XM_017024662.1:c.194A>G, XM_011524831.2:c.194A>G, XM_011524831.1:c.194A>G, XM_017024665.2:c.92A>G, XM_017024665.1:c.92A>G, XM_011524836.2:c.194A>G, XM_011524836.1:c.194A>G, XM_005257385.2:c.194A>G, XM_005257385.1:c.194A>G, XM_017024667.2:c.194A>G, XM_017024667.1:c.194A>G, XM_011524833.2:c.194A>G, XM_011524833.1:c.194A>G, XM_011524834.2:c.92A>G, XM_011524834.1:c.92A>G, XM_047436107.1:c.92A>G, XM_047436110.1:c.92A>G, XM_047436111.1:c.194A>G, XM_047436106.1:c.194A>G, XM_047436109.1:c.194A>G, XM_047436119.1:c.194A>G, XM_047436120.1:c.92A>G, XM_047436124.1:c.92A>G, XM_047436125.1:c.92A>G, XM_047436126.1:c.92A>G, XM_047436108.1:c.194A>G, XM_047436113.1:c.92A>G, XM_047436115.1:c.194A>G, XM_047436114.1:c.92A>G, XM_047436116.1:c.194A>G, XM_047436117.1:c.194A>G, XM_047436121.1:c.92A>G, XM_047436122.1:c.92A>G, XM_047436123.1:c.194A>G, XM_047436112.1:c.92A>G, XM_047436118.1:c.194A>G, NP_056109.1:p.Asn65Ser, NP_001005207.1:p.Asn65Ser, NP_001307916.1:p.Asn31Ser, NP_001307917.1:p.Asn65Ser, NP_001307918.1:p.Asn65Ser, NP_001340013.1:p.Asn65Ser, NP_001340015.1:p.Asn65Ser, NP_001340011.1:p.Asn31Ser, XP_011523134.1:p.Asn65Ser, XP_016880152.1:p.Asn65Ser, XP_016880158.1:p.Asn31Ser, XP_016880159.1:p.Asn31Ser, XP_016880151.1:p.Asn65Ser, XP_011523133.1:p.Asn65Ser, XP_016880154.1:p.Asn31Ser, XP_011523138.1:p.Asn65Ser, XP_005257442.1:p.Asn65Ser, XP_016880156.1:p.Asn65Ser, XP_011523135.1:p.Asn65Ser, XP_011523136.1:p.Asn31Ser, XP_047292063.1:p.Asn31Ser, XP_047292066.1:p.Asn31Ser, XP_047292067.1:p.Asn65Ser, XP_047292062.1:p.Asn65Ser, XP_047292065.1:p.Asn65Ser, XP_047292075.1:p.Asn65Ser, XP_047292076.1:p.Asn31Ser, XP_047292080.1:p.Asn31Ser, XP_047292081.1:p.Asn31Ser, XP_047292082.1:p.Asn31Ser, XP_047292064.1:p.Asn65Ser, XP_047292069.1:p.Asn31Ser, XP_047292071.1:p.Asn65Ser, XP_047292070.1:p.Asn31Ser, XP_047292072.1:p.Asn65Ser, XP_047292073.1:p.Asn65Ser, XP_047292077.1:p.Asn31Ser, XP_047292078.1:p.Asn31Ser, XP_047292079.1:p.Asn65Ser, XP_047292068.1:p.Asn31Ser, XP_047292074.1:p.Asn65Ser

                8.

                rs1480459291 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>T [Show Flanks]
                  Chromosome:
                  17:59079837 (GRCh38)
                  17:57157198 (GRCh37)
                  Canonical SPDI:
                  NC_000017.11:59079836:C:T
                  Gene:
                  TRIM37 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant,missense_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  T=0./0 (ALFA)
                  T=0.000004/1 (TOPMED)
                  HGVS:
                  NC_000017.11:g.59079837C>T, NC_000017.10:g.57157198C>T, NG_009298.1:g.32069G>A, NM_015294.6:c.533G>A, NM_015294.5:c.533G>A, NM_015294.4:c.533G>A, NM_015294.3:c.533G>A, NM_001005207.5:c.533G>A, NM_001005207.4:c.533G>A, NM_001005207.3:c.533G>A, NM_001005207.2:c.533G>A, NM_001320990.3:c.167G>A, NM_001320990.2:c.167G>A, NM_001320990.1:c.167G>A, NM_001320987.3:c.431G>A, NM_001320987.2:c.431G>A, NM_001320987.1:c.431G>A, NM_001320988.3:c.533G>A, NM_001320988.2:c.533G>A, NM_001320988.1:c.533G>A, NM_001320989.3:c.533G>A, NM_001320989.2:c.533G>A, NM_001320989.1:c.533G>A, NR_148346.2:n.952G>A, NR_148346.1:n.1036G>A, NM_001353084.2:c.533G>A, NM_001353084.1:c.533G>A, NM_001353083.2:c.-220G>A, NM_001353083.1:c.-220G>A, NM_001353086.2:c.533G>A, NM_001353086.1:c.533G>A, NR_148347.2:n.850G>A, NR_148347.1:n.934G>A, NM_001353082.2:c.431G>A, NM_001353082.1:c.431G>A, NM_001353085.2:c.71G>A, NM_001353085.1:c.71G>A, XM_011524832.3:c.533G>A, XM_011524832.2:c.533G>A, XM_011524832.1:c.533G>A, XM_017024663.3:c.533G>A, XM_017024663.2:c.533G>A, XM_017024663.1:c.533G>A, XM_017024669.3:c.431G>A, XM_017024669.2:c.431G>A, XM_017024669.1:c.431G>A, XM_017024670.3:c.431G>A, XM_017024670.2:c.431G>A, XM_017024670.1:c.431G>A, XM_017024662.2:c.533G>A, XM_017024662.1:c.533G>A, XM_011524831.2:c.533G>A, XM_011524831.1:c.533G>A, XM_017024665.2:c.431G>A, XM_017024665.1:c.431G>A, XM_011524836.2:c.533G>A, XM_011524836.1:c.533G>A, XM_005257385.2:c.533G>A, XM_005257385.1:c.533G>A, XM_017024667.2:c.533G>A, XM_017024667.1:c.533G>A, XM_011524833.2:c.533G>A, XM_011524833.1:c.533G>A, XM_011524834.2:c.431G>A, XM_011524834.1:c.431G>A, XM_047436107.1:c.431G>A, XM_047436110.1:c.431G>A, XM_047436111.1:c.533G>A, XM_047436106.1:c.533G>A, XM_047436109.1:c.533G>A, XM_047436119.1:c.533G>A, XM_047436120.1:c.431G>A, XM_047436124.1:c.431G>A, XM_047436125.1:c.431G>A, XM_047436126.1:c.431G>A, XM_047436108.1:c.533G>A, XM_047436113.1:c.431G>A, XM_047436115.1:c.533G>A, XM_047436114.1:c.431G>A, XM_047436116.1:c.533G>A, XM_047436117.1:c.533G>A, XM_047436121.1:c.431G>A, XM_047436122.1:c.431G>A, XM_047436123.1:c.533G>A, XM_047436112.1:c.431G>A, XM_047436118.1:c.533G>A, NP_056109.1:p.Arg178His, NP_001005207.1:p.Arg178His, NP_001307919.1:p.Arg56His, NP_001307916.1:p.Arg144His, NP_001307917.1:p.Arg178His, NP_001307918.1:p.Arg178His, NP_001340013.1:p.Arg178His, NP_001340015.1:p.Arg178His, NP_001340011.1:p.Arg144His, NP_001340014.1:p.Arg24His, XP_011523134.1:p.Arg178His, XP_016880152.1:p.Arg178His, XP_016880158.1:p.Arg144His, XP_016880159.1:p.Arg144His, XP_016880151.1:p.Arg178His, XP_011523133.1:p.Arg178His, XP_016880154.1:p.Arg144His, XP_011523138.1:p.Arg178His, XP_005257442.1:p.Arg178His, XP_016880156.1:p.Arg178His, XP_011523135.1:p.Arg178His, XP_011523136.1:p.Arg144His, XP_047292063.1:p.Arg144His, XP_047292066.1:p.Arg144His, XP_047292067.1:p.Arg178His, XP_047292062.1:p.Arg178His, XP_047292065.1:p.Arg178His, XP_047292075.1:p.Arg178His, XP_047292076.1:p.Arg144His, XP_047292080.1:p.Arg144His, XP_047292081.1:p.Arg144His, XP_047292082.1:p.Arg144His, XP_047292064.1:p.Arg178His, XP_047292069.1:p.Arg144His, XP_047292071.1:p.Arg178His, XP_047292070.1:p.Arg144His, XP_047292072.1:p.Arg178His, XP_047292073.1:p.Arg178His, XP_047292077.1:p.Arg144His, XP_047292078.1:p.Arg144His, XP_047292079.1:p.Arg178His, XP_047292068.1:p.Arg144His, XP_047292074.1:p.Arg178His

                  9.

                  rs1480325266 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>G,T [Show Flanks]
                    Chromosome:
                    17:59047789 (GRCh38)
                    17:57125150 (GRCh37)
                    Canonical SPDI:
                    NC_000017.11:59047788:C:G,NC_000017.11:59047788:C:T
                    Gene:
                    TRIM37 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant,coding_sequence_variant,missense_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0./0 (ALFA)
                    HGVS:
                    NC_000017.11:g.59047789C>G, NC_000017.11:g.59047789C>T, NC_000017.10:g.57125150C>G, NC_000017.10:g.57125150C>T, NG_009298.1:g.64117G>C, NG_009298.1:g.64117G>A, NM_015294.6:c.1561G>C, NM_015294.6:c.1561G>A, NM_015294.5:c.1561G>C, NM_015294.5:c.1561G>A, NM_015294.4:c.1561G>C, NM_015294.4:c.1561G>A, NM_015294.3:c.1561G>C, NM_015294.3:c.1561G>A, NM_001005207.5:c.1561G>C, NM_001005207.5:c.1561G>A, NM_001005207.4:c.1561G>C, NM_001005207.4:c.1561G>A, NM_001005207.3:c.1561G>C, NM_001005207.3:c.1561G>A, NM_001005207.2:c.1561G>C, NM_001005207.2:c.1561G>A, NM_001320990.3:c.1195G>C, NM_001320990.3:c.1195G>A, NM_001320990.2:c.1195G>C, NM_001320990.2:c.1195G>A, NM_001320990.1:c.1195G>C, NM_001320990.1:c.1195G>A, NM_001320987.3:c.1459G>C, NM_001320987.3:c.1459G>A, NM_001320987.2:c.1459G>C, NM_001320987.2:c.1459G>A, NM_001320987.1:c.1459G>C, NM_001320987.1:c.1459G>A, NM_001320988.3:c.1561G>C, NM_001320988.3:c.1561G>A, NM_001320988.2:c.1561G>C, NM_001320988.2:c.1561G>A, NM_001320988.1:c.1561G>C, NM_001320988.1:c.1561G>A, NM_001320989.3:c.1561G>C, NM_001320989.3:c.1561G>A, NM_001320989.2:c.1561G>C, NM_001320989.2:c.1561G>A, NM_001320989.1:c.1561G>C, NM_001320989.1:c.1561G>A, NR_148346.2:n.1980G>C, NR_148346.2:n.1980G>A, NR_148346.1:n.2064G>C, NR_148346.1:n.2064G>A, NM_001353084.2:c.1561G>C, NM_001353084.2:c.1561G>A, NM_001353084.1:c.1561G>C, NM_001353084.1:c.1561G>A, NM_001353083.2:c.826G>C, NM_001353083.2:c.826G>A, NM_001353083.1:c.826G>C, NM_001353083.1:c.826G>A, NM_001353086.2:c.1510G>C, NM_001353086.2:c.1510G>A, NM_001353086.1:c.1510G>C, NM_001353086.1:c.1510G>A, NR_148347.2:n.1878G>C, NR_148347.2:n.1878G>A, NR_148347.1:n.1962G>C, NR_148347.1:n.1962G>A, NM_001353082.2:c.1459G>C, NM_001353082.2:c.1459G>A, NM_001353082.1:c.1459G>C, NM_001353082.1:c.1459G>A, NM_001353085.2:c.1099G>C, NM_001353085.2:c.1099G>A, NM_001353085.1:c.1099G>C, NM_001353085.1:c.1099G>A, XM_011524832.3:c.1561G>C, XM_011524832.3:c.1561G>A, XM_011524832.2:c.1561G>C, XM_011524832.2:c.1561G>A, XM_011524832.1:c.1561G>C, XM_011524832.1:c.1561G>A, XM_017024663.3:c.1561G>C, XM_017024663.3:c.1561G>A, XM_017024663.2:c.1561G>C, XM_017024663.2:c.1561G>A, XM_017024663.1:c.1561G>C, XM_017024663.1:c.1561G>A, XM_017024669.3:c.1408G>C, XM_017024669.3:c.1408G>A, XM_017024669.2:c.1408G>C, XM_017024669.2:c.1408G>A, XM_017024669.1:c.1408G>C, XM_017024669.1:c.1408G>A, XM_017024670.3:c.1459G>C, XM_017024670.3:c.1459G>A, XM_017024670.2:c.1459G>C, XM_017024670.2:c.1459G>A, XM_017024670.1:c.1459G>C, XM_017024670.1:c.1459G>A, XM_017024673.3:c.826G>C, XM_017024673.3:c.826G>A, XM_017024673.2:c.826G>C, XM_017024673.2:c.826G>A, XM_017024673.1:c.826G>C, XM_017024673.1:c.826G>A, XM_017024662.2:c.1561G>C, XM_017024662.2:c.1561G>A, XM_017024662.1:c.1561G>C, XM_017024662.1:c.1561G>A, XM_011524831.2:c.1561G>C, XM_011524831.2:c.1561G>A, XM_011524831.1:c.1561G>C, XM_011524831.1:c.1561G>A, XM_017024665.2:c.1459G>C, XM_017024665.2:c.1459G>A, XM_017024665.1:c.1459G>C, XM_017024665.1:c.1459G>A, XM_011524836.2:c.1561G>C, XM_011524836.2:c.1561G>A, XM_011524836.1:c.1561G>C, XM_011524836.1:c.1561G>A, XM_005257385.2:c.1561G>C, XM_005257385.2:c.1561G>A, XM_005257385.1:c.1561G>C, XM_005257385.1:c.1561G>A, XM_017024667.2:c.1510G>C, XM_017024667.2:c.1510G>A, XM_017024667.1:c.1510G>C, XM_017024667.1:c.1510G>A, XM_011524833.2:c.1510G>C, XM_011524833.2:c.1510G>A, XM_011524833.1:c.1510G>C, XM_011524833.1:c.1510G>A, XM_011524834.2:c.1459G>C, XM_011524834.2:c.1459G>A, XM_011524834.1:c.1459G>C, XM_011524834.1:c.1459G>A, XM_047436107.1:c.1459G>C, XM_047436107.1:c.1459G>A, XM_047436110.1:c.1459G>C, XM_047436110.1:c.1459G>A, XM_047436111.1:c.1561G>C, XM_047436111.1:c.1561G>A, XM_047436106.1:c.1510G>C, XM_047436106.1:c.1510G>A, XM_047436109.1:c.1561G>C, XM_047436109.1:c.1561G>A, XM_047436119.1:c.1510G>C, XM_047436119.1:c.1510G>A, XM_047436120.1:c.1459G>C, XM_047436120.1:c.1459G>A, XM_047436124.1:c.1408G>C, XM_047436124.1:c.1408G>A, XM_047436125.1:c.1408G>C, XM_047436125.1:c.1408G>A, XM_047436126.1:c.1459G>C, XM_047436126.1:c.1459G>A, XM_047436108.1:c.1510G>C, XM_047436108.1:c.1510G>A, XM_047436113.1:c.1459G>C, XM_047436113.1:c.1459G>A, XM_047436115.1:c.1561G>C, XM_047436115.1:c.1561G>A, XM_047436114.1:c.1459G>C, XM_047436114.1:c.1459G>A, XM_047436116.1:c.1561G>C, XM_047436116.1:c.1561G>A, XM_047436117.1:c.1510G>C, XM_047436117.1:c.1510G>A, XM_047436121.1:c.1459G>C, XM_047436121.1:c.1459G>A, XM_047436122.1:c.1459G>C, XM_047436122.1:c.1459G>A, XM_047436123.1:c.1561G>C, XM_047436123.1:c.1561G>A, XM_047436112.1:c.1408G>C, XM_047436112.1:c.1408G>A, XM_047436118.1:c.1561G>C, XM_047436118.1:c.1561G>A, NP_056109.1:p.Asp521His, NP_056109.1:p.Asp521Asn, NP_001005207.1:p.Asp521His, NP_001005207.1:p.Asp521Asn, NP_001307919.1:p.Asp399His, NP_001307919.1:p.Asp399Asn, NP_001307916.1:p.Asp487His, NP_001307916.1:p.Asp487Asn, NP_001307917.1:p.Asp521His, NP_001307917.1:p.Asp521Asn, NP_001307918.1:p.Asp521His, NP_001307918.1:p.Asp521Asn, NP_001340013.1:p.Asp521His, NP_001340013.1:p.Asp521Asn, NP_001340012.1:p.Asp276His, NP_001340012.1:p.Asp276Asn, NP_001340015.1:p.Asp504His, NP_001340015.1:p.Asp504Asn, NP_001340011.1:p.Asp487His, NP_001340011.1:p.Asp487Asn, NP_001340014.1:p.Asp367His, NP_001340014.1:p.Asp367Asn, XP_011523134.1:p.Asp521His, XP_011523134.1:p.Asp521Asn, XP_016880152.1:p.Asp521His, XP_016880152.1:p.Asp521Asn, XP_016880158.1:p.Asp470His, XP_016880158.1:p.Asp470Asn, XP_016880159.1:p.Asp487His, XP_016880159.1:p.Asp487Asn, XP_016880162.1:p.Asp276His, XP_016880162.1:p.Asp276Asn, XP_016880151.1:p.Asp521His, XP_016880151.1:p.Asp521Asn, XP_011523133.1:p.Asp521His, XP_011523133.1:p.Asp521Asn, XP_016880154.1:p.Asp487His, XP_016880154.1:p.Asp487Asn, XP_011523138.1:p.Asp521His, XP_011523138.1:p.Asp521Asn, XP_005257442.1:p.Asp521His, XP_005257442.1:p.Asp521Asn, XP_016880156.1:p.Asp504His, XP_016880156.1:p.Asp504Asn, XP_011523135.1:p.Asp504His, XP_011523135.1:p.Asp504Asn, XP_011523136.1:p.Asp487His, XP_011523136.1:p.Asp487Asn, XP_047292063.1:p.Asp487His, XP_047292063.1:p.Asp487Asn, XP_047292066.1:p.Asp487His, XP_047292066.1:p.Asp487Asn, XP_047292067.1:p.Asp521His, XP_047292067.1:p.Asp521Asn, XP_047292062.1:p.Asp504His, XP_047292062.1:p.Asp504Asn, XP_047292065.1:p.Asp521His, XP_047292065.1:p.Asp521Asn, XP_047292075.1:p.Asp504His, XP_047292075.1:p.Asp504Asn, XP_047292076.1:p.Asp487His, XP_047292076.1:p.Asp487Asn, XP_047292080.1:p.Asp470His, XP_047292080.1:p.Asp470Asn, XP_047292081.1:p.Asp470His, XP_047292081.1:p.Asp470Asn, XP_047292082.1:p.Asp487His, XP_047292082.1:p.Asp487Asn, XP_047292064.1:p.Asp504His, XP_047292064.1:p.Asp504Asn, XP_047292069.1:p.Asp487His, XP_047292069.1:p.Asp487Asn, XP_047292071.1:p.Asp521His, XP_047292071.1:p.Asp521Asn, XP_047292070.1:p.Asp487His, XP_047292070.1:p.Asp487Asn, XP_047292072.1:p.Asp521His, XP_047292072.1:p.Asp521Asn, XP_047292073.1:p.Asp504His, XP_047292073.1:p.Asp504Asn, XP_047292077.1:p.Asp487His, XP_047292077.1:p.Asp487Asn, XP_047292078.1:p.Asp487His, XP_047292078.1:p.Asp487Asn, XP_047292079.1:p.Asp521His, XP_047292079.1:p.Asp521Asn, XP_047292068.1:p.Asp470His, XP_047292068.1:p.Asp470Asn, XP_047292074.1:p.Asp521His, XP_047292074.1:p.Asp521Asn

                    10.

                    rs1475495551 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>A [Show Flanks]
                      Chromosome:
                      17:59012410 (GRCh38)
                      17:57089771 (GRCh37)
                      Canonical SPDI:
                      NC_000017.11:59012409:C:A
                      Gene:
                      TRIM37 (Varview)
                      Functional Consequence:
                      non_coding_transcript_variant,coding_sequence_variant,missense_variant
                      Validated:
                      by frequency
                      MAF:
                      A=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000017.11:g.59012410C>A, NC_000017.10:g.57089771C>A, NG_009298.1:g.99496G>T, NM_015294.6:c.2613G>T, NM_015294.5:c.2613G>T, NM_015294.4:c.2613G>T, NM_015294.3:c.2613G>T, NM_001005207.5:c.2613G>T, NM_001005207.4:c.2613G>T, NM_001005207.3:c.2613G>T, NM_001005207.2:c.2613G>T, NM_001320990.3:c.2247G>T, NM_001320990.2:c.2247G>T, NM_001320990.1:c.2247G>T, NM_001320987.3:c.2511G>T, NM_001320987.2:c.2511G>T, NM_001320987.1:c.2511G>T, NM_001320988.3:c.2613G>T, NM_001320988.2:c.2613G>T, NM_001320988.1:c.2613G>T, NM_001320989.3:c.2613G>T, NM_001320989.2:c.2613G>T, NM_001320989.1:c.2613G>T, NR_148346.2:n.3032G>T, NR_148346.1:n.3116G>T, NM_001353084.2:c.2613G>T, NM_001353084.1:c.2613G>T, NM_001353083.2:c.1878G>T, NM_001353083.1:c.1878G>T, NM_001353086.2:c.2562G>T, NM_001353086.1:c.2562G>T, NR_148347.2:n.2930G>T, NR_148347.1:n.3014G>T, NM_001353082.2:c.2511G>T, NM_001353082.1:c.2511G>T, NM_001353085.2:c.2151G>T, NM_001353085.1:c.2151G>T, XM_011524832.3:c.2613G>T, XM_011524832.2:c.2613G>T, XM_011524832.1:c.2613G>T, XM_017024663.3:c.2613G>T, XM_017024663.2:c.2613G>T, XM_017024663.1:c.2613G>T, XM_017024669.3:c.2460G>T, XM_017024669.2:c.2460G>T, XM_017024669.1:c.2460G>T, XM_017024670.3:c.2511G>T, XM_017024670.2:c.2511G>T, XM_017024670.1:c.2511G>T, XM_017024673.3:c.1878G>T, XM_017024673.2:c.1878G>T, XM_017024673.1:c.1878G>T, XM_017024662.2:c.2613G>T, XM_017024662.1:c.2613G>T, XM_011524831.2:c.2613G>T, XM_011524831.1:c.2613G>T, XM_017024665.2:c.2511G>T, XM_017024665.1:c.2511G>T, XM_011524836.2:c.2613G>T, XM_011524836.1:c.2613G>T, XM_005257385.2:c.2613G>T, XM_005257385.1:c.2613G>T, XM_017024667.2:c.2562G>T, XM_017024667.1:c.2562G>T, XM_011524833.2:c.2562G>T, XM_011524833.1:c.2562G>T, XM_011524834.2:c.2511G>T, XM_011524834.1:c.2511G>T, XM_047436107.1:c.2511G>T, XM_047436110.1:c.2511G>T, XM_047436111.1:c.2613G>T, XM_047436106.1:c.2562G>T, XM_047436109.1:c.2484G>T, XM_047436119.1:c.2433G>T, XM_047436120.1:c.2382G>T, XM_047436124.1:c.2460G>T, XM_047436125.1:c.2331G>T, XM_047436126.1:c.2382G>T, XM_047436108.1:c.2562G>T, XM_047436113.1:c.2511G>T, XM_047436115.1:c.2484G>T, XM_047436114.1:c.2511G>T, XM_047436116.1:c.2484G>T, XM_047436117.1:c.2562G>T, XM_047436121.1:c.2511G>T, XM_047436122.1:c.2382G>T, XM_047436123.1:c.2484G>T, XM_047436112.1:c.2460G>T, XM_047436118.1:c.2484G>T, NP_056109.1:p.Gln871His, NP_001005207.1:p.Gln871His, NP_001307919.1:p.Gln749His, NP_001307916.1:p.Gln837His, NP_001307917.1:p.Gln871His, NP_001307918.1:p.Gln871His, NP_001340013.1:p.Gln871His, NP_001340012.1:p.Gln626His, NP_001340015.1:p.Gln854His, NP_001340011.1:p.Gln837His, NP_001340014.1:p.Gln717His, XP_011523134.1:p.Gln871His, XP_016880152.1:p.Gln871His, XP_016880158.1:p.Gln820His, XP_016880159.1:p.Gln837His, XP_016880162.1:p.Gln626His, XP_016880151.1:p.Gln871His, XP_011523133.1:p.Gln871His, XP_016880154.1:p.Gln837His, XP_011523138.1:p.Gln871His, XP_005257442.1:p.Gln871His, XP_016880156.1:p.Gln854His, XP_011523135.1:p.Gln854His, XP_011523136.1:p.Gln837His, XP_047292063.1:p.Gln837His, XP_047292066.1:p.Gln837His, XP_047292067.1:p.Gln871His, XP_047292062.1:p.Gln854His, XP_047292065.1:p.Gln828His, XP_047292075.1:p.Gln811His, XP_047292076.1:p.Gln794His, XP_047292080.1:p.Gln820His, XP_047292081.1:p.Gln777His, XP_047292082.1:p.Gln794His, XP_047292064.1:p.Gln854His, XP_047292069.1:p.Gln837His, XP_047292071.1:p.Gln828His, XP_047292070.1:p.Gln837His, XP_047292072.1:p.Gln828His, XP_047292073.1:p.Gln854His, XP_047292077.1:p.Gln837His, XP_047292078.1:p.Gln794His, XP_047292079.1:p.Gln828His, XP_047292068.1:p.Gln820His, XP_047292074.1:p.Gln828His

                      11.

                      rs1472556210 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>C [Show Flanks]
                        Chromosome:
                        17:59015786 (GRCh38)
                        17:57093147 (GRCh37)
                        Canonical SPDI:
                        NC_000017.11:59015785:G:C
                        Gene:
                        TRIM37 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant,coding_sequence_variant,missense_variant
                        Validated:
                        by frequency
                        MAF:
                        C=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000017.11:g.59015786G>C, NC_000017.10:g.57093147G>C, NG_009298.1:g.96120C>G, NM_015294.6:c.2400C>G, NM_015294.5:c.2400C>G, NM_015294.4:c.2400C>G, NM_015294.3:c.2400C>G, NM_001005207.5:c.2400C>G, NM_001005207.4:c.2400C>G, NM_001005207.3:c.2400C>G, NM_001005207.2:c.2400C>G, NM_001320990.3:c.2034C>G, NM_001320990.2:c.2034C>G, NM_001320990.1:c.2034C>G, NM_001320987.3:c.2298C>G, NM_001320987.2:c.2298C>G, NM_001320987.1:c.2298C>G, NM_001320988.3:c.2400C>G, NM_001320988.2:c.2400C>G, NM_001320988.1:c.2400C>G, NM_001320989.3:c.2400C>G, NM_001320989.2:c.2400C>G, NM_001320989.1:c.2400C>G, NR_148346.2:n.2819C>G, NR_148346.1:n.2903C>G, NM_001353084.2:c.2400C>G, NM_001353084.1:c.2400C>G, NM_001353083.2:c.1665C>G, NM_001353083.1:c.1665C>G, NM_001353086.2:c.2349C>G, NM_001353086.1:c.2349C>G, NR_148347.2:n.2717C>G, NR_148347.1:n.2801C>G, NM_001353082.2:c.2298C>G, NM_001353082.1:c.2298C>G, NM_001353085.2:c.1938C>G, NM_001353085.1:c.1938C>G, XM_011524832.3:c.2400C>G, XM_011524832.2:c.2400C>G, XM_011524832.1:c.2400C>G, XM_017024663.3:c.2400C>G, XM_017024663.2:c.2400C>G, XM_017024663.1:c.2400C>G, XM_017024669.3:c.2247C>G, XM_017024669.2:c.2247C>G, XM_017024669.1:c.2247C>G, XM_017024670.3:c.2298C>G, XM_017024670.2:c.2298C>G, XM_017024670.1:c.2298C>G, XM_017024673.3:c.1665C>G, XM_017024673.2:c.1665C>G, XM_017024673.1:c.1665C>G, XM_017024662.2:c.2400C>G, XM_017024662.1:c.2400C>G, XM_011524831.2:c.2400C>G, XM_011524831.1:c.2400C>G, XM_017024665.2:c.2298C>G, XM_017024665.1:c.2298C>G, XM_011524836.2:c.2400C>G, XM_011524836.1:c.2400C>G, XM_005257385.2:c.2400C>G, XM_005257385.1:c.2400C>G, XM_017024667.2:c.2349C>G, XM_017024667.1:c.2349C>G, XM_011524833.2:c.2349C>G, XM_011524833.1:c.2349C>G, XM_011524834.2:c.2298C>G, XM_011524834.1:c.2298C>G, XM_047436107.1:c.2298C>G, XM_047436110.1:c.2298C>G, XM_047436111.1:c.2400C>G, XM_047436106.1:c.2349C>G, XM_047436109.1:c.2271C>G, XM_047436119.1:c.2220C>G, XM_047436120.1:c.2169C>G, XM_047436124.1:c.2247C>G, XM_047436125.1:c.2118C>G, XM_047436126.1:c.2169C>G, XM_047436108.1:c.2349C>G, XM_047436113.1:c.2298C>G, XM_047436115.1:c.2271C>G, XM_047436114.1:c.2298C>G, XM_047436116.1:c.2271C>G, XM_047436117.1:c.2349C>G, XM_047436121.1:c.2298C>G, XM_047436122.1:c.2169C>G, XM_047436123.1:c.2271C>G, XM_047436112.1:c.2247C>G, XM_047436118.1:c.2271C>G, NP_056109.1:p.Ser800Arg, NP_001005207.1:p.Ser800Arg, NP_001307919.1:p.Ser678Arg, NP_001307916.1:p.Ser766Arg, NP_001307917.1:p.Ser800Arg, NP_001307918.1:p.Ser800Arg, NP_001340013.1:p.Ser800Arg, NP_001340012.1:p.Ser555Arg, NP_001340015.1:p.Ser783Arg, NP_001340011.1:p.Ser766Arg, NP_001340014.1:p.Ser646Arg, XP_011523134.1:p.Ser800Arg, XP_016880152.1:p.Ser800Arg, XP_016880158.1:p.Ser749Arg, XP_016880159.1:p.Ser766Arg, XP_016880162.1:p.Ser555Arg, XP_016880151.1:p.Ser800Arg, XP_011523133.1:p.Ser800Arg, XP_016880154.1:p.Ser766Arg, XP_011523138.1:p.Ser800Arg, XP_005257442.1:p.Ser800Arg, XP_016880156.1:p.Ser783Arg, XP_011523135.1:p.Ser783Arg, XP_011523136.1:p.Ser766Arg, XP_047292063.1:p.Ser766Arg, XP_047292066.1:p.Ser766Arg, XP_047292067.1:p.Ser800Arg, XP_047292062.1:p.Ser783Arg, XP_047292065.1:p.Ser757Arg, XP_047292075.1:p.Ser740Arg, XP_047292076.1:p.Ser723Arg, XP_047292080.1:p.Ser749Arg, XP_047292081.1:p.Ser706Arg, XP_047292082.1:p.Ser723Arg, XP_047292064.1:p.Ser783Arg, XP_047292069.1:p.Ser766Arg, XP_047292071.1:p.Ser757Arg, XP_047292070.1:p.Ser766Arg, XP_047292072.1:p.Ser757Arg, XP_047292073.1:p.Ser783Arg, XP_047292077.1:p.Ser766Arg, XP_047292078.1:p.Ser723Arg, XP_047292079.1:p.Ser757Arg, XP_047292068.1:p.Ser749Arg, XP_047292074.1:p.Ser757Arg

                        12.

                        rs1472442837 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          17:59031956 (GRCh38)
                          17:57109317 (GRCh37)
                          Canonical SPDI:
                          NC_000017.11:59031955:T:C
                          Gene:
                          TRIM37 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant,coding_sequence_variant,missense_variant
                          Validated:
                          by frequency
                          MAF:
                          C=0.000008/2 (GnomAD_exomes)
                          HGVS:
                          NC_000017.11:g.59031956T>C, NC_000017.10:g.57109317T>C, NG_009298.1:g.79950A>G, NM_015294.6:c.1888A>G, NM_015294.5:c.1888A>G, NM_015294.4:c.1888A>G, NM_015294.3:c.1888A>G, NM_001005207.5:c.1888A>G, NM_001005207.4:c.1888A>G, NM_001005207.3:c.1888A>G, NM_001005207.2:c.1888A>G, NM_001320990.3:c.1522A>G, NM_001320990.2:c.1522A>G, NM_001320990.1:c.1522A>G, NM_001320987.3:c.1786A>G, NM_001320987.2:c.1786A>G, NM_001320987.1:c.1786A>G, NM_001320988.3:c.1888A>G, NM_001320988.2:c.1888A>G, NM_001320988.1:c.1888A>G, NM_001320989.3:c.1888A>G, NM_001320989.2:c.1888A>G, NM_001320989.1:c.1888A>G, NR_148346.2:n.2307A>G, NR_148346.1:n.2391A>G, NM_001353084.2:c.1888A>G, NM_001353084.1:c.1888A>G, NM_001353083.2:c.1153A>G, NM_001353083.1:c.1153A>G, NM_001353086.2:c.1837A>G, NM_001353086.1:c.1837A>G, NR_148347.2:n.2205A>G, NR_148347.1:n.2289A>G, NM_001353082.2:c.1786A>G, NM_001353082.1:c.1786A>G, NM_001353085.2:c.1426A>G, NM_001353085.1:c.1426A>G, XM_011524832.3:c.1888A>G, XM_011524832.2:c.1888A>G, XM_011524832.1:c.1888A>G, XM_017024663.3:c.1888A>G, XM_017024663.2:c.1888A>G, XM_017024663.1:c.1888A>G, XM_017024669.3:c.1735A>G, XM_017024669.2:c.1735A>G, XM_017024669.1:c.1735A>G, XM_017024670.3:c.1786A>G, XM_017024670.2:c.1786A>G, XM_017024670.1:c.1786A>G, XM_017024673.3:c.1153A>G, XM_017024673.2:c.1153A>G, XM_017024673.1:c.1153A>G, XM_017024662.2:c.1888A>G, XM_017024662.1:c.1888A>G, XM_011524831.2:c.1888A>G, XM_011524831.1:c.1888A>G, XM_017024665.2:c.1786A>G, XM_017024665.1:c.1786A>G, XM_011524836.2:c.1888A>G, XM_011524836.1:c.1888A>G, XM_005257385.2:c.1888A>G, XM_005257385.1:c.1888A>G, XM_017024667.2:c.1837A>G, XM_017024667.1:c.1837A>G, XM_011524833.2:c.1837A>G, XM_011524833.1:c.1837A>G, XM_011524834.2:c.1786A>G, XM_011524834.1:c.1786A>G, XM_047436107.1:c.1786A>G, XM_047436110.1:c.1786A>G, XM_047436111.1:c.1888A>G, XM_047436106.1:c.1837A>G, XM_047436109.1:c.1888A>G, XM_047436119.1:c.1837A>G, XM_047436120.1:c.1786A>G, XM_047436124.1:c.1735A>G, XM_047436125.1:c.1735A>G, XM_047436126.1:c.1786A>G, XM_047436108.1:c.1837A>G, XM_047436113.1:c.1786A>G, XM_047436115.1:c.1888A>G, XM_047436114.1:c.1786A>G, XM_047436116.1:c.1888A>G, XM_047436117.1:c.1837A>G, XM_047436121.1:c.1786A>G, XM_047436122.1:c.1786A>G, XM_047436123.1:c.1888A>G, XM_047436112.1:c.1735A>G, XM_047436118.1:c.1888A>G, NP_056109.1:p.Ser630Gly, NP_001005207.1:p.Ser630Gly, NP_001307919.1:p.Ser508Gly, NP_001307916.1:p.Ser596Gly, NP_001307917.1:p.Ser630Gly, NP_001307918.1:p.Ser630Gly, NP_001340013.1:p.Ser630Gly, NP_001340012.1:p.Ser385Gly, NP_001340015.1:p.Ser613Gly, NP_001340011.1:p.Ser596Gly, NP_001340014.1:p.Ser476Gly, XP_011523134.1:p.Ser630Gly, XP_016880152.1:p.Ser630Gly, XP_016880158.1:p.Ser579Gly, XP_016880159.1:p.Ser596Gly, XP_016880162.1:p.Ser385Gly, XP_016880151.1:p.Ser630Gly, XP_011523133.1:p.Ser630Gly, XP_016880154.1:p.Ser596Gly, XP_011523138.1:p.Ser630Gly, XP_005257442.1:p.Ser630Gly, XP_016880156.1:p.Ser613Gly, XP_011523135.1:p.Ser613Gly, XP_011523136.1:p.Ser596Gly, XP_047292063.1:p.Ser596Gly, XP_047292066.1:p.Ser596Gly, XP_047292067.1:p.Ser630Gly, XP_047292062.1:p.Ser613Gly, XP_047292065.1:p.Ser630Gly, XP_047292075.1:p.Ser613Gly, XP_047292076.1:p.Ser596Gly, XP_047292080.1:p.Ser579Gly, XP_047292081.1:p.Ser579Gly, XP_047292082.1:p.Ser596Gly, XP_047292064.1:p.Ser613Gly, XP_047292069.1:p.Ser596Gly, XP_047292071.1:p.Ser630Gly, XP_047292070.1:p.Ser596Gly, XP_047292072.1:p.Ser630Gly, XP_047292073.1:p.Ser613Gly, XP_047292077.1:p.Ser596Gly, XP_047292078.1:p.Ser596Gly, XP_047292079.1:p.Ser630Gly, XP_047292068.1:p.Ser579Gly, XP_047292074.1:p.Ser630Gly

                          13.

                          rs1472147846 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            17:59049346 (GRCh38)
                            17:57126707 (GRCh37)
                            Canonical SPDI:
                            NC_000017.11:59049345:T:C
                            Gene:
                            TRIM37 (Varview)
                            Functional Consequence:
                            synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000004/1 (TOPMED)
                            C=0.000007/1 (GnomAD)
                            HGVS:
                            NC_000017.11:g.59049346T>C, NC_000017.10:g.57126707T>C, NG_009298.1:g.62560A>G, NM_015294.6:c.1362A>G, NM_015294.5:c.1362A>G, NM_015294.4:c.1362A>G, NM_015294.3:c.1362A>G, NM_001005207.5:c.1362A>G, NM_001005207.4:c.1362A>G, NM_001005207.3:c.1362A>G, NM_001005207.2:c.1362A>G, NM_001320990.3:c.996A>G, NM_001320990.2:c.996A>G, NM_001320990.1:c.996A>G, NM_001320987.3:c.1260A>G, NM_001320987.2:c.1260A>G, NM_001320987.1:c.1260A>G, NM_001320988.3:c.1362A>G, NM_001320988.2:c.1362A>G, NM_001320988.1:c.1362A>G, NM_001320989.3:c.1362A>G, NM_001320989.2:c.1362A>G, NM_001320989.1:c.1362A>G, NR_148346.2:n.1781A>G, NR_148346.1:n.1865A>G, NM_001353084.2:c.1362A>G, NM_001353084.1:c.1362A>G, NM_001353083.2:c.627A>G, NM_001353083.1:c.627A>G, NM_001353086.2:c.1311A>G, NM_001353086.1:c.1311A>G, NR_148347.2:n.1679A>G, NR_148347.1:n.1763A>G, NM_001353082.2:c.1260A>G, NM_001353082.1:c.1260A>G, NM_001353085.2:c.900A>G, NM_001353085.1:c.900A>G, XM_011524832.3:c.1362A>G, XM_011524832.2:c.1362A>G, XM_011524832.1:c.1362A>G, XM_017024663.3:c.1362A>G, XM_017024663.2:c.1362A>G, XM_017024663.1:c.1362A>G, XM_017024669.3:c.1209A>G, XM_017024669.2:c.1209A>G, XM_017024669.1:c.1209A>G, XM_017024670.3:c.1260A>G, XM_017024670.2:c.1260A>G, XM_017024670.1:c.1260A>G, XM_017024673.3:c.627A>G, XM_017024673.2:c.627A>G, XM_017024673.1:c.627A>G, XM_017024662.2:c.1362A>G, XM_017024662.1:c.1362A>G, XM_011524831.2:c.1362A>G, XM_011524831.1:c.1362A>G, XM_017024665.2:c.1260A>G, XM_017024665.1:c.1260A>G, XM_011524836.2:c.1362A>G, XM_011524836.1:c.1362A>G, XM_005257385.2:c.1362A>G, XM_005257385.1:c.1362A>G, XM_017024667.2:c.1311A>G, XM_017024667.1:c.1311A>G, XM_011524833.2:c.1311A>G, XM_011524833.1:c.1311A>G, XM_011524834.2:c.1260A>G, XM_011524834.1:c.1260A>G, XM_047436107.1:c.1260A>G, XM_047436110.1:c.1260A>G, XM_047436111.1:c.1362A>G, XM_047436106.1:c.1311A>G, XM_047436109.1:c.1362A>G, XM_047436119.1:c.1311A>G, XM_047436120.1:c.1260A>G, XM_047436124.1:c.1209A>G, XM_047436125.1:c.1209A>G, XM_047436126.1:c.1260A>G, XM_047436108.1:c.1311A>G, XM_047436113.1:c.1260A>G, XM_047436115.1:c.1362A>G, XM_047436114.1:c.1260A>G, XM_047436116.1:c.1362A>G, XM_047436117.1:c.1311A>G, XM_047436121.1:c.1260A>G, XM_047436122.1:c.1260A>G, XM_047436123.1:c.1362A>G, XM_047436112.1:c.1209A>G, XM_047436118.1:c.1362A>G

                            14.

                            rs1471107105 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C,G [Show Flanks]
                              Chromosome:
                              17:59012344 (GRCh38)
                              17:57089705 (GRCh37)
                              Canonical SPDI:
                              NC_000017.11:59012343:T:C,NC_000017.11:59012343:T:G
                              Gene:
                              TRIM37 (Varview)
                              Functional Consequence:
                              synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0.000031/1 (ALFA)
                              C=0.000007/1 (GnomAD)
                              C=0.000008/2 (TOPMED)
                              HGVS:
                              NC_000017.11:g.59012344T>C, NC_000017.11:g.59012344T>G, NC_000017.10:g.57089705T>C, NC_000017.10:g.57089705T>G, NG_009298.1:g.99562A>G, NG_009298.1:g.99562A>C, NM_015294.6:c.2679A>G, NM_015294.6:c.2679A>C, NM_015294.5:c.2679A>G, NM_015294.5:c.2679A>C, NM_015294.4:c.2679A>G, NM_015294.4:c.2679A>C, NM_015294.3:c.2679A>G, NM_015294.3:c.2679A>C, NM_001005207.5:c.2679A>G, NM_001005207.5:c.2679A>C, NM_001005207.4:c.2679A>G, NM_001005207.4:c.2679A>C, NM_001005207.3:c.2679A>G, NM_001005207.3:c.2679A>C, NM_001005207.2:c.2679A>G, NM_001005207.2:c.2679A>C, NM_001320990.3:c.2313A>G, NM_001320990.3:c.2313A>C, NM_001320990.2:c.2313A>G, NM_001320990.2:c.2313A>C, NM_001320990.1:c.2313A>G, NM_001320990.1:c.2313A>C, NM_001320987.3:c.2577A>G, NM_001320987.3:c.2577A>C, NM_001320987.2:c.2577A>G, NM_001320987.2:c.2577A>C, NM_001320987.1:c.2577A>G, NM_001320987.1:c.2577A>C, NM_001320988.3:c.2679A>G, NM_001320988.3:c.2679A>C, NM_001320988.2:c.2679A>G, NM_001320988.2:c.2679A>C, NM_001320988.1:c.2679A>G, NM_001320988.1:c.2679A>C, NM_001320989.3:c.2679A>G, NM_001320989.3:c.2679A>C, NM_001320989.2:c.2679A>G, NM_001320989.2:c.2679A>C, NM_001320989.1:c.2679A>G, NM_001320989.1:c.2679A>C, NR_148346.2:n.3098A>G, NR_148346.2:n.3098A>C, NR_148346.1:n.3182A>G, NR_148346.1:n.3182A>C, NM_001353084.2:c.2679A>G, NM_001353084.2:c.2679A>C, NM_001353084.1:c.2679A>G, NM_001353084.1:c.2679A>C, NM_001353083.2:c.1944A>G, NM_001353083.2:c.1944A>C, NM_001353083.1:c.1944A>G, NM_001353083.1:c.1944A>C, NM_001353086.2:c.2628A>G, NM_001353086.2:c.2628A>C, NM_001353086.1:c.2628A>G, NM_001353086.1:c.2628A>C, NR_148347.2:n.2996A>G, NR_148347.2:n.2996A>C, NR_148347.1:n.3080A>G, NR_148347.1:n.3080A>C, NM_001353082.2:c.2577A>G, NM_001353082.2:c.2577A>C, NM_001353082.1:c.2577A>G, NM_001353082.1:c.2577A>C, NM_001353085.2:c.2217A>G, NM_001353085.2:c.2217A>C, NM_001353085.1:c.2217A>G, NM_001353085.1:c.2217A>C, XM_011524832.3:c.2679A>G, XM_011524832.3:c.2679A>C, XM_011524832.2:c.2679A>G, XM_011524832.2:c.2679A>C, XM_011524832.1:c.2679A>G, XM_011524832.1:c.2679A>C, XM_017024663.3:c.2679A>G, XM_017024663.3:c.2679A>C, XM_017024663.2:c.2679A>G, XM_017024663.2:c.2679A>C, XM_017024663.1:c.2679A>G, XM_017024663.1:c.2679A>C, XM_017024669.3:c.2526A>G, XM_017024669.3:c.2526A>C, XM_017024669.2:c.2526A>G, XM_017024669.2:c.2526A>C, XM_017024669.1:c.2526A>G, XM_017024669.1:c.2526A>C, XM_017024670.3:c.2577A>G, XM_017024670.3:c.2577A>C, XM_017024670.2:c.2577A>G, XM_017024670.2:c.2577A>C, XM_017024670.1:c.2577A>G, XM_017024670.1:c.2577A>C, XM_017024673.3:c.1944A>G, XM_017024673.3:c.1944A>C, XM_017024673.2:c.1944A>G, XM_017024673.2:c.1944A>C, XM_017024673.1:c.1944A>G, XM_017024673.1:c.1944A>C, XM_017024662.2:c.2679A>G, XM_017024662.2:c.2679A>C, XM_017024662.1:c.2679A>G, XM_017024662.1:c.2679A>C, XM_011524831.2:c.2679A>G, XM_011524831.2:c.2679A>C, XM_011524831.1:c.2679A>G, XM_011524831.1:c.2679A>C, XM_017024665.2:c.2577A>G, XM_017024665.2:c.2577A>C, XM_017024665.1:c.2577A>G, XM_017024665.1:c.2577A>C, XM_011524836.2:c.2679A>G, XM_011524836.2:c.2679A>C, XM_011524836.1:c.2679A>G, XM_011524836.1:c.2679A>C, XM_005257385.2:c.2679A>G, XM_005257385.2:c.2679A>C, XM_005257385.1:c.2679A>G, XM_005257385.1:c.2679A>C, XM_017024667.2:c.2628A>G, XM_017024667.2:c.2628A>C, XM_017024667.1:c.2628A>G, XM_017024667.1:c.2628A>C, XM_011524833.2:c.2628A>G, XM_011524833.2:c.2628A>C, XM_011524833.1:c.2628A>G, XM_011524833.1:c.2628A>C, XM_011524834.2:c.2577A>G, XM_011524834.2:c.2577A>C, XM_011524834.1:c.2577A>G, XM_011524834.1:c.2577A>C, XM_047436107.1:c.2577A>G, XM_047436107.1:c.2577A>C, XM_047436110.1:c.2577A>G, XM_047436110.1:c.2577A>C, XM_047436111.1:c.2679A>G, XM_047436111.1:c.2679A>C, XM_047436106.1:c.2628A>G, XM_047436106.1:c.2628A>C, XM_047436109.1:c.2550A>G, XM_047436109.1:c.2550A>C, XM_047436119.1:c.2499A>G, XM_047436119.1:c.2499A>C, XM_047436120.1:c.2448A>G, XM_047436120.1:c.2448A>C, XM_047436124.1:c.2526A>G, XM_047436124.1:c.2526A>C, XM_047436125.1:c.2397A>G, XM_047436125.1:c.2397A>C, XM_047436126.1:c.2448A>G, XM_047436126.1:c.2448A>C, XM_047436108.1:c.2628A>G, XM_047436108.1:c.2628A>C, XM_047436113.1:c.2577A>G, XM_047436113.1:c.2577A>C, XM_047436115.1:c.2550A>G, XM_047436115.1:c.2550A>C, XM_047436114.1:c.2577A>G, XM_047436114.1:c.2577A>C, XM_047436116.1:c.2550A>G, XM_047436116.1:c.2550A>C, XM_047436117.1:c.2628A>G, XM_047436117.1:c.2628A>C, XM_047436121.1:c.2577A>G, XM_047436121.1:c.2577A>C, XM_047436122.1:c.2448A>G, XM_047436122.1:c.2448A>C, XM_047436123.1:c.2550A>G, XM_047436123.1:c.2550A>C, XM_047436112.1:c.2526A>G, XM_047436112.1:c.2526A>C, XM_047436118.1:c.2550A>G, XM_047436118.1:c.2550A>C

                              15.

                              rs1470999393 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                17:59084053 (GRCh38)
                                17:57161414 (GRCh37)
                                Canonical SPDI:
                                NC_000017.11:59084052:G:A
                                Gene:
                                TRIM37 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,non_coding_transcript_variant,intron_variant,5_prime_UTR_variant,synonymous_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency
                                MAF:
                                A=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000017.11:g.59084053G>A, NC_000017.10:g.57161414G>A, NG_009298.1:g.27853C>T, NM_015294.6:c.318C>T, NM_015294.5:c.318C>T, NM_015294.4:c.318C>T, NM_015294.3:c.318C>T, NM_001005207.5:c.318C>T, NM_001005207.4:c.318C>T, NM_001005207.3:c.318C>T, NM_001005207.2:c.318C>T, NM_001320990.3:c.-49C>T, NM_001320990.2:c.-49C>T, NM_001320990.1:c.-49C>T, NM_001320987.3:c.216C>T, NM_001320987.2:c.216C>T, NM_001320987.1:c.216C>T, NM_001320988.3:c.318C>T, NM_001320988.2:c.318C>T, NM_001320988.1:c.318C>T, NM_001320989.3:c.318C>T, NM_001320989.2:c.318C>T, NM_001320989.1:c.318C>T, NR_148346.2:n.737C>T, NR_148346.1:n.821C>T, NM_001353084.2:c.318C>T, NM_001353084.1:c.318C>T, NM_001353083.2:c.-435C>T, NM_001353083.1:c.-435C>T, NM_001353086.2:c.318C>T, NM_001353086.1:c.318C>T, NR_148347.2:n.635C>T, NR_148347.1:n.719C>T, NM_001353082.2:c.216C>T, NM_001353082.1:c.216C>T, XM_011524832.3:c.318C>T, XM_011524832.2:c.318C>T, XM_011524832.1:c.318C>T, XM_017024663.3:c.318C>T, XM_017024663.2:c.318C>T, XM_017024663.1:c.318C>T, XM_017024669.3:c.216C>T, XM_017024669.2:c.216C>T, XM_017024669.1:c.216C>T, XM_017024670.3:c.216C>T, XM_017024670.2:c.216C>T, XM_017024670.1:c.216C>T, XM_017024662.2:c.318C>T, XM_017024662.1:c.318C>T, XM_011524831.2:c.318C>T, XM_011524831.1:c.318C>T, XM_017024665.2:c.216C>T, XM_017024665.1:c.216C>T, XM_011524836.2:c.318C>T, XM_011524836.1:c.318C>T, XM_005257385.2:c.318C>T, XM_005257385.1:c.318C>T, XM_017024667.2:c.318C>T, XM_017024667.1:c.318C>T, XM_011524833.2:c.318C>T, XM_011524833.1:c.318C>T, XM_011524834.2:c.216C>T, XM_011524834.1:c.216C>T, XM_047436107.1:c.216C>T, XM_047436110.1:c.216C>T, XM_047436111.1:c.318C>T, XM_047436106.1:c.318C>T, XM_047436109.1:c.318C>T, XM_047436119.1:c.318C>T, XM_047436120.1:c.216C>T, XM_047436124.1:c.216C>T, XM_047436125.1:c.216C>T, XM_047436126.1:c.216C>T, XM_047436108.1:c.318C>T, XM_047436113.1:c.216C>T, XM_047436115.1:c.318C>T, XM_047436114.1:c.216C>T, XM_047436116.1:c.318C>T, XM_047436117.1:c.318C>T, XM_047436121.1:c.216C>T, XM_047436122.1:c.216C>T, XM_047436123.1:c.318C>T, XM_047436112.1:c.216C>T, XM_047436118.1:c.318C>T

                                16.

                                rs1470987924 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>T [Show Flanks]
                                  Chromosome:
                                  17:59070892 (GRCh38)
                                  17:57148253 (GRCh37)
                                  Canonical SPDI:
                                  NC_000017.11:59070891:A:T
                                  Gene:
                                  TRIM37 (Varview)
                                  Functional Consequence:
                                  non_coding_transcript_variant,coding_sequence_variant,missense_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  T=0.000004/1 (TOPMED)
                                  T=0.000014/2 (GnomAD)
                                  T=0.000016/4 (GnomAD_exomes)
                                  HGVS:
                                  NC_000017.11:g.59070892A>T, NC_000017.10:g.57148253A>T, NG_009298.1:g.41014T>A, NM_015294.6:c.740T>A, NM_015294.5:c.740T>A, NM_015294.4:c.740T>A, NM_015294.3:c.740T>A, NM_001005207.5:c.740T>A, NM_001005207.4:c.740T>A, NM_001005207.3:c.740T>A, NM_001005207.2:c.740T>A, NM_001320990.3:c.374T>A, NM_001320990.2:c.374T>A, NM_001320990.1:c.374T>A, NM_001320987.3:c.638T>A, NM_001320987.2:c.638T>A, NM_001320987.1:c.638T>A, NM_001320988.3:c.740T>A, NM_001320988.2:c.740T>A, NM_001320988.1:c.740T>A, NM_001320989.3:c.740T>A, NM_001320989.2:c.740T>A, NM_001320989.1:c.740T>A, NR_148346.2:n.1159T>A, NR_148346.1:n.1243T>A, NM_001353084.2:c.740T>A, NM_001353084.1:c.740T>A, NM_001353083.2:c.5T>A, NM_001353083.1:c.5T>A, NM_001353086.2:c.740T>A, NM_001353086.1:c.740T>A, NR_148347.2:n.1057T>A, NR_148347.1:n.1141T>A, NM_001353082.2:c.638T>A, NM_001353082.1:c.638T>A, NM_001353085.2:c.278T>A, NM_001353085.1:c.278T>A, XM_011524832.3:c.740T>A, XM_011524832.2:c.740T>A, XM_011524832.1:c.740T>A, XM_017024663.3:c.740T>A, XM_017024663.2:c.740T>A, XM_017024663.1:c.740T>A, XM_017024669.3:c.638T>A, XM_017024669.2:c.638T>A, XM_017024669.1:c.638T>A, XM_017024670.3:c.638T>A, XM_017024670.2:c.638T>A, XM_017024670.1:c.638T>A, XM_017024673.3:c.5T>A, XM_017024673.2:c.5T>A, XM_017024673.1:c.5T>A, XM_017024662.2:c.740T>A, XM_017024662.1:c.740T>A, XM_011524831.2:c.740T>A, XM_011524831.1:c.740T>A, XM_017024665.2:c.638T>A, XM_017024665.1:c.638T>A, XM_011524836.2:c.740T>A, XM_011524836.1:c.740T>A, XM_005257385.2:c.740T>A, XM_005257385.1:c.740T>A, XM_017024667.2:c.740T>A, XM_017024667.1:c.740T>A, XM_011524833.2:c.740T>A, XM_011524833.1:c.740T>A, XM_011524834.2:c.638T>A, XM_011524834.1:c.638T>A, XM_047436107.1:c.638T>A, XM_047436110.1:c.638T>A, XM_047436111.1:c.740T>A, XM_047436106.1:c.740T>A, XM_047436109.1:c.740T>A, XM_047436119.1:c.740T>A, XM_047436120.1:c.638T>A, XM_047436124.1:c.638T>A, XM_047436125.1:c.638T>A, XM_047436126.1:c.638T>A, XM_047436108.1:c.740T>A, XM_047436113.1:c.638T>A, XM_047436115.1:c.740T>A, XM_047436114.1:c.638T>A, XM_047436116.1:c.740T>A, XM_047436117.1:c.740T>A, XM_047436121.1:c.638T>A, XM_047436122.1:c.638T>A, XM_047436123.1:c.740T>A, XM_047436112.1:c.638T>A, XM_047436118.1:c.740T>A, NP_056109.1:p.Met247Lys, NP_001005207.1:p.Met247Lys, NP_001307919.1:p.Met125Lys, NP_001307916.1:p.Met213Lys, NP_001307917.1:p.Met247Lys, NP_001307918.1:p.Met247Lys, NP_001340013.1:p.Met247Lys, NP_001340012.1:p.Met2Lys, NP_001340015.1:p.Met247Lys, NP_001340011.1:p.Met213Lys, NP_001340014.1:p.Met93Lys, XP_011523134.1:p.Met247Lys, XP_016880152.1:p.Met247Lys, XP_016880158.1:p.Met213Lys, XP_016880159.1:p.Met213Lys, XP_016880162.1:p.Met2Lys, XP_016880151.1:p.Met247Lys, XP_011523133.1:p.Met247Lys, XP_016880154.1:p.Met213Lys, XP_011523138.1:p.Met247Lys, XP_005257442.1:p.Met247Lys, XP_016880156.1:p.Met247Lys, XP_011523135.1:p.Met247Lys, XP_011523136.1:p.Met213Lys, XP_047292063.1:p.Met213Lys, XP_047292066.1:p.Met213Lys, XP_047292067.1:p.Met247Lys, XP_047292062.1:p.Met247Lys, XP_047292065.1:p.Met247Lys, XP_047292075.1:p.Met247Lys, XP_047292076.1:p.Met213Lys, XP_047292080.1:p.Met213Lys, XP_047292081.1:p.Met213Lys, XP_047292082.1:p.Met213Lys, XP_047292064.1:p.Met247Lys, XP_047292069.1:p.Met213Lys, XP_047292071.1:p.Met247Lys, XP_047292070.1:p.Met213Lys, XP_047292072.1:p.Met247Lys, XP_047292073.1:p.Met247Lys, XP_047292077.1:p.Met213Lys, XP_047292078.1:p.Met213Lys, XP_047292079.1:p.Met247Lys, XP_047292068.1:p.Met213Lys, XP_047292074.1:p.Met247Lys

                                  17.

                                  rs1470896066 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    17:59081157 (GRCh38)
                                    17:57158518 (GRCh37)
                                    Canonical SPDI:
                                    NC_000017.11:59081156:A:G
                                    Gene:
                                    TRIM37 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant,synonymous_variant,genic_upstream_transcript_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    G=0.000004/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000017.11:g.59081157A>G, NC_000017.10:g.57158518A>G, NG_009298.1:g.30749T>C, NM_015294.6:c.432T>C, NM_015294.5:c.432T>C, NM_015294.4:c.432T>C, NM_015294.3:c.432T>C, NM_001005207.5:c.432T>C, NM_001005207.4:c.432T>C, NM_001005207.3:c.432T>C, NM_001005207.2:c.432T>C, NM_001320990.3:c.66T>C, NM_001320990.2:c.66T>C, NM_001320990.1:c.66T>C, NM_001320987.3:c.330T>C, NM_001320987.2:c.330T>C, NM_001320987.1:c.330T>C, NM_001320988.3:c.432T>C, NM_001320988.2:c.432T>C, NM_001320988.1:c.432T>C, NM_001320989.3:c.432T>C, NM_001320989.2:c.432T>C, NM_001320989.1:c.432T>C, NR_148346.2:n.851T>C, NR_148346.1:n.935T>C, NM_001353084.2:c.432T>C, NM_001353084.1:c.432T>C, NM_001353083.2:c.-321T>C, NM_001353083.1:c.-321T>C, NM_001353086.2:c.432T>C, NM_001353086.1:c.432T>C, NR_148347.2:n.749T>C, NR_148347.1:n.833T>C, NM_001353082.2:c.330T>C, NM_001353082.1:c.330T>C, NM_001353085.2:c.-31T>C, NM_001353085.1:c.-31T>C, XM_011524832.3:c.432T>C, XM_011524832.2:c.432T>C, XM_011524832.1:c.432T>C, XM_017024663.3:c.432T>C, XM_017024663.2:c.432T>C, XM_017024663.1:c.432T>C, XM_017024669.3:c.330T>C, XM_017024669.2:c.330T>C, XM_017024669.1:c.330T>C, XM_017024670.3:c.330T>C, XM_017024670.2:c.330T>C, XM_017024670.1:c.330T>C, XM_017024662.2:c.432T>C, XM_017024662.1:c.432T>C, XM_011524831.2:c.432T>C, XM_011524831.1:c.432T>C, XM_017024665.2:c.330T>C, XM_017024665.1:c.330T>C, XM_011524836.2:c.432T>C, XM_011524836.1:c.432T>C, XM_005257385.2:c.432T>C, XM_005257385.1:c.432T>C, XM_017024667.2:c.432T>C, XM_017024667.1:c.432T>C, XM_011524833.2:c.432T>C, XM_011524833.1:c.432T>C, XM_011524834.2:c.330T>C, XM_011524834.1:c.330T>C, XM_047436107.1:c.330T>C, XM_047436110.1:c.330T>C, XM_047436111.1:c.432T>C, XM_047436106.1:c.432T>C, XM_047436109.1:c.432T>C, XM_047436119.1:c.432T>C, XM_047436120.1:c.330T>C, XM_047436124.1:c.330T>C, XM_047436125.1:c.330T>C, XM_047436126.1:c.330T>C, XM_047436108.1:c.432T>C, XM_047436113.1:c.330T>C, XM_047436115.1:c.432T>C, XM_047436114.1:c.330T>C, XM_047436116.1:c.432T>C, XM_047436117.1:c.432T>C, XM_047436121.1:c.330T>C, XM_047436122.1:c.330T>C, XM_047436123.1:c.432T>C, XM_047436112.1:c.330T>C, XM_047436118.1:c.432T>C

                                    18.

                                    rs1470754495 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>T [Show Flanks]
                                      Chromosome:
                                      17:59041860 (GRCh38)
                                      17:57119221 (GRCh37)
                                      Canonical SPDI:
                                      NC_000017.11:59041859:A:T
                                      Gene:
                                      TRIM37 (Varview)
                                      Functional Consequence:
                                      stop_gained,non_coding_transcript_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      T=0./0 (ALFA)
                                      HGVS:
                                      NC_000017.11:g.59041860A>T, NC_000017.10:g.57119221A>T, NG_009298.1:g.70046T>A, NM_015294.6:c.1706T>A, NM_015294.5:c.1706T>A, NM_015294.4:c.1706T>A, NM_015294.3:c.1706T>A, NM_001005207.5:c.1706T>A, NM_001005207.4:c.1706T>A, NM_001005207.3:c.1706T>A, NM_001005207.2:c.1706T>A, NM_001320990.3:c.1340T>A, NM_001320990.2:c.1340T>A, NM_001320990.1:c.1340T>A, NM_001320987.3:c.1604T>A, NM_001320987.2:c.1604T>A, NM_001320987.1:c.1604T>A, NM_001320988.3:c.1706T>A, NM_001320988.2:c.1706T>A, NM_001320988.1:c.1706T>A, NM_001320989.3:c.1706T>A, NM_001320989.2:c.1706T>A, NM_001320989.1:c.1706T>A, NR_148346.2:n.2125T>A, NR_148346.1:n.2209T>A, NM_001353084.2:c.1706T>A, NM_001353084.1:c.1706T>A, NM_001353083.2:c.971T>A, NM_001353083.1:c.971T>A, NM_001353086.2:c.1655T>A, NM_001353086.1:c.1655T>A, NR_148347.2:n.2023T>A, NR_148347.1:n.2107T>A, NM_001353082.2:c.1604T>A, NM_001353082.1:c.1604T>A, NM_001353085.2:c.1244T>A, NM_001353085.1:c.1244T>A, XM_011524832.3:c.1706T>A, XM_011524832.2:c.1706T>A, XM_011524832.1:c.1706T>A, XM_017024663.3:c.1706T>A, XM_017024663.2:c.1706T>A, XM_017024663.1:c.1706T>A, XM_017024669.3:c.1553T>A, XM_017024669.2:c.1553T>A, XM_017024669.1:c.1553T>A, XM_017024670.3:c.1604T>A, XM_017024670.2:c.1604T>A, XM_017024670.1:c.1604T>A, XM_017024673.3:c.971T>A, XM_017024673.2:c.971T>A, XM_017024673.1:c.971T>A, XM_017024662.2:c.1706T>A, XM_017024662.1:c.1706T>A, XM_011524831.2:c.1706T>A, XM_011524831.1:c.1706T>A, XM_017024665.2:c.1604T>A, XM_017024665.1:c.1604T>A, XM_011524836.2:c.1706T>A, XM_011524836.1:c.1706T>A, XM_005257385.2:c.1706T>A, XM_005257385.1:c.1706T>A, XM_017024667.2:c.1655T>A, XM_017024667.1:c.1655T>A, XM_011524833.2:c.1655T>A, XM_011524833.1:c.1655T>A, XM_011524834.2:c.1604T>A, XM_011524834.1:c.1604T>A, XM_047436107.1:c.1604T>A, XM_047436110.1:c.1604T>A, XM_047436111.1:c.1706T>A, XM_047436106.1:c.1655T>A, XM_047436109.1:c.1706T>A, XM_047436119.1:c.1655T>A, XM_047436120.1:c.1604T>A, XM_047436124.1:c.1553T>A, XM_047436125.1:c.1553T>A, XM_047436126.1:c.1604T>A, XM_047436108.1:c.1655T>A, XM_047436113.1:c.1604T>A, XM_047436115.1:c.1706T>A, XM_047436114.1:c.1604T>A, XM_047436116.1:c.1706T>A, XM_047436117.1:c.1655T>A, XM_047436121.1:c.1604T>A, XM_047436122.1:c.1604T>A, XM_047436123.1:c.1706T>A, XM_047436112.1:c.1553T>A, XM_047436118.1:c.1706T>A, NP_056109.1:p.Leu569Ter, NP_001005207.1:p.Leu569Ter, NP_001307919.1:p.Leu447Ter, NP_001307916.1:p.Leu535Ter, NP_001307917.1:p.Leu569Ter, NP_001307918.1:p.Leu569Ter, NP_001340013.1:p.Leu569Ter, NP_001340012.1:p.Leu324Ter, NP_001340015.1:p.Leu552Ter, NP_001340011.1:p.Leu535Ter, NP_001340014.1:p.Leu415Ter, XP_011523134.1:p.Leu569Ter, XP_016880152.1:p.Leu569Ter, XP_016880158.1:p.Leu518Ter, XP_016880159.1:p.Leu535Ter, XP_016880162.1:p.Leu324Ter, XP_016880151.1:p.Leu569Ter, XP_011523133.1:p.Leu569Ter, XP_016880154.1:p.Leu535Ter, XP_011523138.1:p.Leu569Ter, XP_005257442.1:p.Leu569Ter, XP_016880156.1:p.Leu552Ter, XP_011523135.1:p.Leu552Ter, XP_011523136.1:p.Leu535Ter, XP_047292063.1:p.Leu535Ter, XP_047292066.1:p.Leu535Ter, XP_047292067.1:p.Leu569Ter, XP_047292062.1:p.Leu552Ter, XP_047292065.1:p.Leu569Ter, XP_047292075.1:p.Leu552Ter, XP_047292076.1:p.Leu535Ter, XP_047292080.1:p.Leu518Ter, XP_047292081.1:p.Leu518Ter, XP_047292082.1:p.Leu535Ter, XP_047292064.1:p.Leu552Ter, XP_047292069.1:p.Leu535Ter, XP_047292071.1:p.Leu569Ter, XP_047292070.1:p.Leu535Ter, XP_047292072.1:p.Leu569Ter, XP_047292073.1:p.Leu552Ter, XP_047292077.1:p.Leu535Ter, XP_047292078.1:p.Leu535Ter, XP_047292079.1:p.Leu569Ter, XP_047292068.1:p.Leu518Ter, XP_047292074.1:p.Leu569Ter

                                      19.

                                      rs1468191938 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        T>C [Show Flanks]
                                        Chromosome:
                                        17:59012393 (GRCh38)
                                        17:57089754 (GRCh37)
                                        Canonical SPDI:
                                        NC_000017.11:59012392:T:C
                                        Gene:
                                        TRIM37 (Varview)
                                        Functional Consequence:
                                        non_coding_transcript_variant,missense_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000007/1 (GnomAD)
                                        C=0.000008/2 (TOPMED)
                                        C=0.000012/3 (GnomAD_exomes)
                                        HGVS:
                                        NC_000017.11:g.59012393T>C, NC_000017.10:g.57089754T>C, NG_009298.1:g.99513A>G, NM_015294.6:c.2630A>G, NM_015294.5:c.2630A>G, NM_015294.4:c.2630A>G, NM_015294.3:c.2630A>G, NM_001005207.5:c.2630A>G, NM_001005207.4:c.2630A>G, NM_001005207.3:c.2630A>G, NM_001005207.2:c.2630A>G, NM_001320990.3:c.2264A>G, NM_001320990.2:c.2264A>G, NM_001320990.1:c.2264A>G, NM_001320987.3:c.2528A>G, NM_001320987.2:c.2528A>G, NM_001320987.1:c.2528A>G, NM_001320988.3:c.2630A>G, NM_001320988.2:c.2630A>G, NM_001320988.1:c.2630A>G, NM_001320989.3:c.2630A>G, NM_001320989.2:c.2630A>G, NM_001320989.1:c.2630A>G, NR_148346.2:n.3049A>G, NR_148346.1:n.3133A>G, NM_001353084.2:c.2630A>G, NM_001353084.1:c.2630A>G, NM_001353083.2:c.1895A>G, NM_001353083.1:c.1895A>G, NM_001353086.2:c.2579A>G, NM_001353086.1:c.2579A>G, NR_148347.2:n.2947A>G, NR_148347.1:n.3031A>G, NM_001353082.2:c.2528A>G, NM_001353082.1:c.2528A>G, NM_001353085.2:c.2168A>G, NM_001353085.1:c.2168A>G, XM_011524832.3:c.2630A>G, XM_011524832.2:c.2630A>G, XM_011524832.1:c.2630A>G, XM_017024663.3:c.2630A>G, XM_017024663.2:c.2630A>G, XM_017024663.1:c.2630A>G, XM_017024669.3:c.2477A>G, XM_017024669.2:c.2477A>G, XM_017024669.1:c.2477A>G, XM_017024670.3:c.2528A>G, XM_017024670.2:c.2528A>G, XM_017024670.1:c.2528A>G, XM_017024673.3:c.1895A>G, XM_017024673.2:c.1895A>G, XM_017024673.1:c.1895A>G, XM_017024662.2:c.2630A>G, XM_017024662.1:c.2630A>G, XM_011524831.2:c.2630A>G, XM_011524831.1:c.2630A>G, XM_017024665.2:c.2528A>G, XM_017024665.1:c.2528A>G, XM_011524836.2:c.2630A>G, XM_011524836.1:c.2630A>G, XM_005257385.2:c.2630A>G, XM_005257385.1:c.2630A>G, XM_017024667.2:c.2579A>G, XM_017024667.1:c.2579A>G, XM_011524833.2:c.2579A>G, XM_011524833.1:c.2579A>G, XM_011524834.2:c.2528A>G, XM_011524834.1:c.2528A>G, XM_047436107.1:c.2528A>G, XM_047436110.1:c.2528A>G, XM_047436111.1:c.2630A>G, XM_047436106.1:c.2579A>G, XM_047436109.1:c.2501A>G, XM_047436119.1:c.2450A>G, XM_047436120.1:c.2399A>G, XM_047436124.1:c.2477A>G, XM_047436125.1:c.2348A>G, XM_047436126.1:c.2399A>G, XM_047436108.1:c.2579A>G, XM_047436113.1:c.2528A>G, XM_047436115.1:c.2501A>G, XM_047436114.1:c.2528A>G, XM_047436116.1:c.2501A>G, XM_047436117.1:c.2579A>G, XM_047436121.1:c.2528A>G, XM_047436122.1:c.2399A>G, XM_047436123.1:c.2501A>G, XM_047436112.1:c.2477A>G, XM_047436118.1:c.2501A>G, NP_056109.1:p.Asn877Ser, NP_001005207.1:p.Asn877Ser, NP_001307919.1:p.Asn755Ser, NP_001307916.1:p.Asn843Ser, NP_001307917.1:p.Asn877Ser, NP_001307918.1:p.Asn877Ser, NP_001340013.1:p.Asn877Ser, NP_001340012.1:p.Asn632Ser, NP_001340015.1:p.Asn860Ser, NP_001340011.1:p.Asn843Ser, NP_001340014.1:p.Asn723Ser, XP_011523134.1:p.Asn877Ser, XP_016880152.1:p.Asn877Ser, XP_016880158.1:p.Asn826Ser, XP_016880159.1:p.Asn843Ser, XP_016880162.1:p.Asn632Ser, XP_016880151.1:p.Asn877Ser, XP_011523133.1:p.Asn877Ser, XP_016880154.1:p.Asn843Ser, XP_011523138.1:p.Asn877Ser, XP_005257442.1:p.Asn877Ser, XP_016880156.1:p.Asn860Ser, XP_011523135.1:p.Asn860Ser, XP_011523136.1:p.Asn843Ser, XP_047292063.1:p.Asn843Ser, XP_047292066.1:p.Asn843Ser, XP_047292067.1:p.Asn877Ser, XP_047292062.1:p.Asn860Ser, XP_047292065.1:p.Asn834Ser, XP_047292075.1:p.Asn817Ser, XP_047292076.1:p.Asn800Ser, XP_047292080.1:p.Asn826Ser, XP_047292081.1:p.Asn783Ser, XP_047292082.1:p.Asn800Ser, XP_047292064.1:p.Asn860Ser, XP_047292069.1:p.Asn843Ser, XP_047292071.1:p.Asn834Ser, XP_047292070.1:p.Asn843Ser, XP_047292072.1:p.Asn834Ser, XP_047292073.1:p.Asn860Ser, XP_047292077.1:p.Asn843Ser, XP_047292078.1:p.Asn800Ser, XP_047292079.1:p.Asn834Ser, XP_047292068.1:p.Asn826Ser, XP_047292074.1:p.Asn834Ser

                                        20.

                                        rs1467761287 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>G [Show Flanks]
                                          Chromosome:
                                          17:59062603 (GRCh38)
                                          17:57139964 (GRCh37)
                                          Canonical SPDI:
                                          NC_000017.11:59062602:T:G
                                          Gene:
                                          TRIM37 (Varview)
                                          Functional Consequence:
                                          non_coding_transcript_variant,missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000012/3 (GnomAD_exomes)
                                          G=0.00003/8 (TOPMED)
                                          G=0.000057/8 (GnomAD)
                                          HGVS:
                                          NC_000017.11:g.59062603T>G, NC_000017.10:g.57139964T>G, NG_009298.1:g.49303A>C, NM_015294.6:c.906A>C, NM_015294.5:c.906A>C, NM_015294.4:c.906A>C, NM_015294.3:c.906A>C, NM_001005207.5:c.906A>C, NM_001005207.4:c.906A>C, NM_001005207.3:c.906A>C, NM_001005207.2:c.906A>C, NM_001320990.3:c.540A>C, NM_001320990.2:c.540A>C, NM_001320990.1:c.540A>C, NM_001320987.3:c.804A>C, NM_001320987.2:c.804A>C, NM_001320987.1:c.804A>C, NM_001320988.3:c.906A>C, NM_001320988.2:c.906A>C, NM_001320988.1:c.906A>C, NM_001320989.3:c.906A>C, NM_001320989.2:c.906A>C, NM_001320989.1:c.906A>C, NR_148346.2:n.1325A>C, NR_148346.1:n.1409A>C, NM_001353084.2:c.906A>C, NM_001353084.1:c.906A>C, NM_001353083.2:c.171A>C, NM_001353083.1:c.171A>C, NM_001353086.2:c.855A>C, NM_001353086.1:c.855A>C, NR_148347.2:n.1223A>C, NR_148347.1:n.1307A>C, NM_001353082.2:c.804A>C, NM_001353082.1:c.804A>C, NM_001353085.2:c.444A>C, NM_001353085.1:c.444A>C, XM_011524832.3:c.906A>C, XM_011524832.2:c.906A>C, XM_011524832.1:c.906A>C, XM_017024663.3:c.906A>C, XM_017024663.2:c.906A>C, XM_017024663.1:c.906A>C, XM_017024669.3:c.753A>C, XM_017024669.2:c.753A>C, XM_017024669.1:c.753A>C, XM_017024670.3:c.804A>C, XM_017024670.2:c.804A>C, XM_017024670.1:c.804A>C, XM_017024673.3:c.171A>C, XM_017024673.2:c.171A>C, XM_017024673.1:c.171A>C, XM_017024662.2:c.906A>C, XM_017024662.1:c.906A>C, XM_011524831.2:c.906A>C, XM_011524831.1:c.906A>C, XM_017024665.2:c.804A>C, XM_017024665.1:c.804A>C, XM_011524836.2:c.906A>C, XM_011524836.1:c.906A>C, XM_005257385.2:c.906A>C, XM_005257385.1:c.906A>C, XM_017024667.2:c.855A>C, XM_017024667.1:c.855A>C, XM_011524833.2:c.855A>C, XM_011524833.1:c.855A>C, XM_011524834.2:c.804A>C, XM_011524834.1:c.804A>C, XM_047436107.1:c.804A>C, XM_047436110.1:c.804A>C, XM_047436111.1:c.906A>C, XM_047436106.1:c.855A>C, XM_047436109.1:c.906A>C, XM_047436119.1:c.855A>C, XM_047436120.1:c.804A>C, XM_047436124.1:c.753A>C, XM_047436125.1:c.753A>C, XM_047436126.1:c.804A>C, XM_047436108.1:c.855A>C, XM_047436113.1:c.804A>C, XM_047436115.1:c.906A>C, XM_047436114.1:c.804A>C, XM_047436116.1:c.906A>C, XM_047436117.1:c.855A>C, XM_047436121.1:c.804A>C, XM_047436122.1:c.804A>C, XM_047436123.1:c.906A>C, XM_047436112.1:c.753A>C, XM_047436118.1:c.906A>C, NP_056109.1:p.Gln302His, NP_001005207.1:p.Gln302His, NP_001307919.1:p.Gln180His, NP_001307916.1:p.Gln268His, NP_001307917.1:p.Gln302His, NP_001307918.1:p.Gln302His, NP_001340013.1:p.Gln302His, NP_001340012.1:p.Gln57His, NP_001340015.1:p.Gln285His, NP_001340011.1:p.Gln268His, NP_001340014.1:p.Gln148His, XP_011523134.1:p.Gln302His, XP_016880152.1:p.Gln302His, XP_016880158.1:p.Gln251His, XP_016880159.1:p.Gln268His, XP_016880162.1:p.Gln57His, XP_016880151.1:p.Gln302His, XP_011523133.1:p.Gln302His, XP_016880154.1:p.Gln268His, XP_011523138.1:p.Gln302His, XP_005257442.1:p.Gln302His, XP_016880156.1:p.Gln285His, XP_011523135.1:p.Gln285His, XP_011523136.1:p.Gln268His, XP_047292063.1:p.Gln268His, XP_047292066.1:p.Gln268His, XP_047292067.1:p.Gln302His, XP_047292062.1:p.Gln285His, XP_047292065.1:p.Gln302His, XP_047292075.1:p.Gln285His, XP_047292076.1:p.Gln268His, XP_047292080.1:p.Gln251His, XP_047292081.1:p.Gln251His, XP_047292082.1:p.Gln268His, XP_047292064.1:p.Gln285His, XP_047292069.1:p.Gln268His, XP_047292071.1:p.Gln302His, XP_047292070.1:p.Gln268His, XP_047292072.1:p.Gln302His, XP_047292073.1:p.Gln285His, XP_047292077.1:p.Gln268His, XP_047292078.1:p.Gln268His, XP_047292079.1:p.Gln302His, XP_047292068.1:p.Gln251His, XP_047292074.1:p.Gln302His

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