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Items: 1 to 20 of 939

1.

rs1490457860 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    1:202276470 (GRCh38)
    1:202245598 (GRCh37)
    Canonical SPDI:
    NC_000001.11:202276469:T:C
    Gene:
    LGR6 (Varview)
    Functional Consequence:
    intron_variant,missense_variant,genic_upstream_transcript_variant,coding_sequence_variant
    HGVS:
    NC_000001.11:g.202276470T>C, NC_000001.10:g.202245598T>C, XM_005245404.4:c.464T>C, XM_005245404.3:c.464T>C, XM_005245404.2:c.464T>C, XM_005245404.1:c.464T>C, XM_011509842.3:c.23T>C, XM_011509842.2:c.23T>C, XM_011509842.1:c.23T>C, XM_011509841.3:c.191T>C, XM_011509841.2:c.191T>C, XM_011509841.1:c.191T>C, NM_021636.3:c.437T>C, NM_021636.2:c.437T>C, XM_011509839.3:c.464T>C, XM_011509839.2:c.464T>C, XM_011509839.1:c.464T>C, XM_011509838.3:c.464T>C, XM_011509838.2:c.464T>C, XM_011509838.1:c.464T>C, XM_011509843.3:c.23T>C, XM_011509843.2:c.23T>C, XM_011509843.1:c.23T>C, XM_011509846.3:c.23T>C, XM_011509846.2:c.23T>C, XM_011509846.1:c.23T>C, NM_001017403.2:c.593T>C, NM_001017403.1:c.593T>C, XM_017001996.2:c.464T>C, XM_017001996.1:c.464T>C, XM_017001997.2:c.191T>C, XM_017001997.1:c.191T>C, XM_047426928.1:c.593T>C, XM_047426929.1:c.593T>C, XM_047426930.1:c.464T>C, XP_005245461.1:p.Ile155Thr, XP_011508144.1:p.Ile8Thr, XP_011508143.1:p.Ile64Thr, NP_067649.2:p.Ile146Thr, XP_011508141.1:p.Ile155Thr, XP_011508140.1:p.Ile155Thr, XP_011508145.1:p.Ile8Thr, XP_011508148.1:p.Ile8Thr, NP_001017403.1:p.Ile198Thr, XP_016857485.1:p.Ile155Thr, XP_016857486.1:p.Ile64Thr, XP_047282884.1:p.Ile198Thr, XP_047282885.1:p.Ile198Thr, XP_047282886.1:p.Ile155Thr

    2.

    rs1489450600 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      1:202309157 (GRCh38)
      1:202278285 (GRCh37)
      Canonical SPDI:
      NC_000001.11:202309156:G:A
      Gene:
      LGR6 (Varview)
      Functional Consequence:
      missense_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa
      MAF:
      A=0./0 (ALFA)
      A=0.000004/1 (TOPMED)
      HGVS:
      NC_000001.11:g.202309157G>A, NC_000001.10:g.202278285G>A, XM_005245404.4:c.1258G>A, XM_005245404.3:c.1258G>A, XM_005245404.2:c.1258G>A, XM_005245404.1:c.1258G>A, XM_011509842.3:c.817G>A, XM_011509842.2:c.817G>A, XM_011509842.1:c.817G>A, XM_011509841.3:c.985G>A, XM_011509841.2:c.985G>A, XM_011509841.1:c.985G>A, NM_021636.3:c.1231G>A, NM_021636.2:c.1231G>A, XM_011509839.3:c.1186G>A, XM_011509839.2:c.1186G>A, XM_011509839.1:c.1186G>A, XM_011509838.3:c.1186G>A, XM_011509838.2:c.1186G>A, XM_011509838.1:c.1186G>A, XM_011509843.3:c.817G>A, XM_011509843.2:c.817G>A, XM_011509843.1:c.817G>A, XM_011509840.3:c.1042G>A, XM_011509840.2:c.1042G>A, XM_011509840.1:c.1042G>A, XM_011509846.3:c.817G>A, XM_011509846.2:c.817G>A, XM_011509846.1:c.817G>A, XM_011509844.3:c.610G>A, XM_011509844.2:c.610G>A, XM_011509844.1:c.610G>A, NM_001017403.2:c.1387G>A, NM_001017403.1:c.1387G>A, XM_017001996.2:c.1114G>A, XM_017001996.1:c.1114G>A, XM_017001997.2:c.985G>A, XM_017001997.1:c.985G>A, NM_001017404.2:c.970G>A, NM_001017404.1:c.970G>A, XM_047426928.1:c.1315G>A, XM_047426929.1:c.1243G>A, XM_047426931.1:c.1171G>A, XM_047426930.1:c.1042G>A, XM_047426932.1:c.898G>A, XP_005245461.1:p.Asp420Asn, XP_011508144.1:p.Asp273Asn, XP_011508143.1:p.Asp329Asn, NP_067649.2:p.Asp411Asn, XP_011508141.1:p.Asp396Asn, XP_011508140.1:p.Asp396Asn, XP_011508145.1:p.Asp273Asn, XP_011508142.1:p.Asp348Asn, XP_011508148.1:p.Asp273Asn, XP_011508146.1:p.Asp204Asn, NP_001017403.1:p.Asp463Asn, XP_016857485.1:p.Asp372Asn, XP_016857486.1:p.Asp329Asn, NP_001017404.1:p.Asp324Asn, XP_047282884.1:p.Asp439Asn, XP_047282885.1:p.Asp415Asn, XP_047282887.1:p.Asp391Asn, XP_047282886.1:p.Asp348Asn, XP_047282888.1:p.Asp300Asn

      3.

      rs1487885420 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>T [Show Flanks]
        Chromosome:
        1:202235923 (GRCh38)
        1:202205051 (GRCh37)
        Canonical SPDI:
        NC_000001.11:202235922:A:T
        Gene:
        LGR6 (Varview), LOC101929388 (Varview)
        Functional Consequence:
        intron_variant,upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,missense_variant,genic_upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.000224/1 (ALFA)
        T=0.000007/1 (GnomAD)
        T=0.000223/1 (Estonian)
        HGVS:
        NC_000001.11:g.202235923A>T, NC_000001.10:g.202205051A>T, XM_005245404.4:c.229A>T, XM_005245404.3:c.229A>T, XM_005245404.2:c.229A>T, XM_005245404.1:c.229A>T, NM_021636.3:c.202A>T, NM_021636.2:c.202A>T, XM_011509839.3:c.229A>T, XM_011509839.2:c.229A>T, XM_011509839.1:c.229A>T, XM_011509838.3:c.229A>T, XM_011509838.2:c.229A>T, XM_011509838.1:c.229A>T, XM_011509840.3:c.229A>T, XM_011509840.2:c.229A>T, XM_011509840.1:c.229A>T, NM_001017403.2:c.358A>T, NM_001017403.1:c.358A>T, XM_017001996.2:c.229A>T, XM_017001996.1:c.229A>T, NM_001017404.2:c.229A>T, NM_001017404.1:c.229A>T, XR_922426.2:n.154T>A, XR_922426.1:n.48T>A, XM_047426928.1:c.358A>T, XM_047426929.1:c.358A>T, XM_047426931.1:c.358A>T, XM_047426930.1:c.229A>T, XM_047426932.1:c.229A>T, XP_005245461.1:p.Met77Leu, NP_067649.2:p.Met68Leu, XP_011508141.1:p.Met77Leu, XP_011508140.1:p.Met77Leu, XP_011508142.1:p.Met77Leu, NP_001017403.1:p.Met120Leu, XP_016857485.1:p.Met77Leu, NP_001017404.1:p.Met77Leu, XP_047282884.1:p.Met120Leu, XP_047282885.1:p.Met120Leu, XP_047282887.1:p.Met120Leu, XP_047282886.1:p.Met77Leu, XP_047282888.1:p.Met77Leu

        4.

        rs1486228523 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          A>G [Show Flanks]
          Chromosome:
          1:202314845 (GRCh38)
          1:202283973 (GRCh37)
          Canonical SPDI:
          NC_000001.11:202314844:A:G
          Gene:
          LGR6 (Varview)
          Functional Consequence:
          synonymous_variant,coding_sequence_variant
          Validated:
          by frequency
          MAF:
          G=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000001.11:g.202314845A>G, NC_000001.10:g.202283973A>G, XM_005245404.4:c.1482A>G, XM_005245404.3:c.1482A>G, XM_005245404.2:c.1482A>G, XM_005245404.1:c.1482A>G, XM_011509842.3:c.1041A>G, XM_011509842.2:c.1041A>G, XM_011509842.1:c.1041A>G, XM_011509841.3:c.1209A>G, XM_011509841.2:c.1209A>G, XM_011509841.1:c.1209A>G, NM_021636.3:c.1455A>G, NM_021636.2:c.1455A>G, XM_011509839.3:c.1410A>G, XM_011509839.2:c.1410A>G, XM_011509839.1:c.1410A>G, XM_011509838.3:c.1410A>G, XM_011509838.2:c.1410A>G, XM_011509838.1:c.1410A>G, XM_011509843.3:c.1041A>G, XM_011509843.2:c.1041A>G, XM_011509843.1:c.1041A>G, XM_011509840.3:c.1266A>G, XM_011509840.2:c.1266A>G, XM_011509840.1:c.1266A>G, XM_011509846.3:c.1041A>G, XM_011509846.2:c.1041A>G, XM_011509846.1:c.1041A>G, XM_011509844.3:c.834A>G, XM_011509844.2:c.834A>G, XM_011509844.1:c.834A>G, NM_001017403.2:c.1611A>G, NM_001017403.1:c.1611A>G, XM_017001996.2:c.1338A>G, XM_017001996.1:c.1338A>G, XM_017001997.2:c.1209A>G, XM_017001997.1:c.1209A>G, NM_001017404.2:c.1194A>G, NM_001017404.1:c.1194A>G, XM_047426928.1:c.1539A>G, XM_047426929.1:c.1467A>G, XM_047426931.1:c.1395A>G, XM_047426930.1:c.1266A>G, XM_047426932.1:c.1122A>G

          5.

          rs1485825696 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            1:202318955 (GRCh38)
            1:202288083 (GRCh37)
            Canonical SPDI:
            NC_000001.11:202318954:A:G
            Gene:
            LGR6 (Varview)
            Functional Consequence:
            synonymous_variant,coding_sequence_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000011/3 (TOPMED)
            G=0.000029/4 (GnomAD)
            HGVS:
            NC_000001.11:g.202318955A>G, NC_000001.10:g.202288083A>G, XM_005245404.4:c.2523A>G, XM_005245404.3:c.2523A>G, XM_005245404.2:c.2523A>G, XM_005245404.1:c.2523A>G, XM_011509842.3:c.2082A>G, XM_011509842.2:c.2082A>G, XM_011509842.1:c.2082A>G, XM_011509841.3:c.2250A>G, XM_011509841.2:c.2250A>G, XM_011509841.1:c.2250A>G, NM_021636.3:c.2496A>G, NM_021636.2:c.2496A>G, XM_011509839.3:c.2451A>G, XM_011509839.2:c.2451A>G, XM_011509839.1:c.2451A>G, XM_011509838.3:c.2451A>G, XM_011509838.2:c.2451A>G, XM_011509838.1:c.2451A>G, XM_011509843.3:c.2082A>G, XM_011509843.2:c.2082A>G, XM_011509843.1:c.2082A>G, XM_011509840.3:c.2307A>G, XM_011509840.2:c.2307A>G, XM_011509840.1:c.2307A>G, XM_011509846.3:c.2082A>G, XM_011509846.2:c.2082A>G, XM_011509846.1:c.2082A>G, XM_011509844.3:c.1875A>G, XM_011509844.2:c.1875A>G, XM_011509844.1:c.1875A>G, NM_001017403.2:c.2652A>G, NM_001017403.1:c.2652A>G, XM_017001996.2:c.2379A>G, XM_017001996.1:c.2379A>G, XM_017001997.2:c.2250A>G, XM_017001997.1:c.2250A>G, NM_001017404.2:c.2235A>G, NM_001017404.1:c.2235A>G, XM_047426928.1:c.2580A>G, XM_047426929.1:c.2508A>G, XM_047426931.1:c.2436A>G, XM_047426930.1:c.2307A>G, XM_047426932.1:c.2163A>G

            6.

            rs1483634886 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              1:202319086 (GRCh38)
              1:202288214 (GRCh37)
              Canonical SPDI:
              NC_000001.11:202319085:C:T
              Gene:
              LGR6 (Varview)
              Functional Consequence:
              coding_sequence_variant,missense_variant
              Validated:
              by frequency
              MAF:
              T=0.000004/1 (GnomAD_exomes)
              HGVS:
              NC_000001.11:g.202319086C>T, NC_000001.10:g.202288214C>T, XM_005245404.4:c.2654C>T, XM_005245404.3:c.2654C>T, XM_005245404.2:c.2654C>T, XM_005245404.1:c.2654C>T, XM_011509842.3:c.2213C>T, XM_011509842.2:c.2213C>T, XM_011509842.1:c.2213C>T, XM_011509841.3:c.2381C>T, XM_011509841.2:c.2381C>T, XM_011509841.1:c.2381C>T, NM_021636.3:c.2627C>T, NM_021636.2:c.2627C>T, XM_011509839.3:c.2582C>T, XM_011509839.2:c.2582C>T, XM_011509839.1:c.2582C>T, XM_011509838.3:c.2582C>T, XM_011509838.2:c.2582C>T, XM_011509838.1:c.2582C>T, XM_011509843.3:c.2213C>T, XM_011509843.2:c.2213C>T, XM_011509843.1:c.2213C>T, XM_011509840.3:c.2438C>T, XM_011509840.2:c.2438C>T, XM_011509840.1:c.2438C>T, XM_011509846.3:c.2213C>T, XM_011509846.2:c.2213C>T, XM_011509846.1:c.2213C>T, XM_011509844.3:c.2006C>T, XM_011509844.2:c.2006C>T, XM_011509844.1:c.2006C>T, NM_001017403.2:c.2783C>T, NM_001017403.1:c.2783C>T, XM_017001996.2:c.2510C>T, XM_017001996.1:c.2510C>T, XM_017001997.2:c.2381C>T, XM_017001997.1:c.2381C>T, NM_001017404.2:c.2366C>T, NM_001017404.1:c.2366C>T, XM_047426928.1:c.2711C>T, XM_047426929.1:c.2639C>T, XM_047426931.1:c.2567C>T, XM_047426930.1:c.2438C>T, XM_047426932.1:c.2294C>T, XP_005245461.1:p.Pro885Leu, XP_011508144.1:p.Pro738Leu, XP_011508143.1:p.Pro794Leu, NP_067649.2:p.Pro876Leu, XP_011508141.1:p.Pro861Leu, XP_011508140.1:p.Pro861Leu, XP_011508145.1:p.Pro738Leu, XP_011508142.1:p.Pro813Leu, XP_011508148.1:p.Pro738Leu, XP_011508146.1:p.Pro669Leu, NP_001017403.1:p.Pro928Leu, XP_016857485.1:p.Pro837Leu, XP_016857486.1:p.Pro794Leu, NP_001017404.1:p.Pro789Leu, XP_047282884.1:p.Pro904Leu, XP_047282885.1:p.Pro880Leu, XP_047282887.1:p.Pro856Leu, XP_047282886.1:p.Pro813Leu, XP_047282888.1:p.Pro765Leu

              7.

              rs1483207568 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                1:202318535 (GRCh38)
                1:202287663 (GRCh37)
                Canonical SPDI:
                NC_000001.11:202318534:C:T
                Gene:
                LGR6 (Varview)
                Functional Consequence:
                coding_sequence_variant,synonymous_variant
                Validated:
                by frequency
                MAF:
                T=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000001.11:g.202318535C>T, NC_000001.10:g.202287663C>T, XM_005245404.4:c.2103C>T, XM_005245404.3:c.2103C>T, XM_005245404.2:c.2103C>T, XM_005245404.1:c.2103C>T, XM_011509842.3:c.1662C>T, XM_011509842.2:c.1662C>T, XM_011509842.1:c.1662C>T, XM_011509841.3:c.1830C>T, XM_011509841.2:c.1830C>T, XM_011509841.1:c.1830C>T, NM_021636.3:c.2076C>T, NM_021636.2:c.2076C>T, XM_011509839.3:c.2031C>T, XM_011509839.2:c.2031C>T, XM_011509839.1:c.2031C>T, XM_011509838.3:c.2031C>T, XM_011509838.2:c.2031C>T, XM_011509838.1:c.2031C>T, XM_011509843.3:c.1662C>T, XM_011509843.2:c.1662C>T, XM_011509843.1:c.1662C>T, XM_011509840.3:c.1887C>T, XM_011509840.2:c.1887C>T, XM_011509840.1:c.1887C>T, XM_011509846.3:c.1662C>T, XM_011509846.2:c.1662C>T, XM_011509846.1:c.1662C>T, XM_011509844.3:c.1455C>T, XM_011509844.2:c.1455C>T, XM_011509844.1:c.1455C>T, NM_001017403.2:c.2232C>T, NM_001017403.1:c.2232C>T, XM_017001996.2:c.1959C>T, XM_017001996.1:c.1959C>T, XM_017001997.2:c.1830C>T, XM_017001997.1:c.1830C>T, NM_001017404.2:c.1815C>T, NM_001017404.1:c.1815C>T, XM_047426928.1:c.2160C>T, XM_047426929.1:c.2088C>T, XM_047426931.1:c.2016C>T, XM_047426930.1:c.1887C>T, XM_047426932.1:c.1743C>T

                8.

                rs1483164207 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A [Show Flanks]
                  Chromosome:
                  1:202318108 (GRCh38)
                  1:202287236 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:202318107:G:A
                  Gene:
                  LGR6 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,missense_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  A=0./0 (ALFA)
                  A=0.000004/1 (TOPMED)
                  A=0.000007/1 (GnomAD)
                  HGVS:
                  NC_000001.11:g.202318108G>A, NC_000001.10:g.202287236G>A, XM_005245404.4:c.1676G>A, XM_005245404.3:c.1676G>A, XM_005245404.2:c.1676G>A, XM_005245404.1:c.1676G>A, XM_011509842.3:c.1235G>A, XM_011509842.2:c.1235G>A, XM_011509842.1:c.1235G>A, XM_011509841.3:c.1403G>A, XM_011509841.2:c.1403G>A, XM_011509841.1:c.1403G>A, NM_021636.3:c.1649G>A, NM_021636.2:c.1649G>A, XM_011509839.3:c.1604G>A, XM_011509839.2:c.1604G>A, XM_011509839.1:c.1604G>A, XM_011509838.3:c.1604G>A, XM_011509838.2:c.1604G>A, XM_011509838.1:c.1604G>A, XM_011509843.3:c.1235G>A, XM_011509843.2:c.1235G>A, XM_011509843.1:c.1235G>A, XM_011509840.3:c.1460G>A, XM_011509840.2:c.1460G>A, XM_011509840.1:c.1460G>A, XM_011509846.3:c.1235G>A, XM_011509846.2:c.1235G>A, XM_011509846.1:c.1235G>A, XM_011509844.3:c.1028G>A, XM_011509844.2:c.1028G>A, XM_011509844.1:c.1028G>A, NM_001017403.2:c.1805G>A, NM_001017403.1:c.1805G>A, XM_017001996.2:c.1532G>A, XM_017001996.1:c.1532G>A, XM_017001997.2:c.1403G>A, XM_017001997.1:c.1403G>A, NM_001017404.2:c.1388G>A, NM_001017404.1:c.1388G>A, XM_047426928.1:c.1733G>A, XM_047426929.1:c.1661G>A, XM_047426931.1:c.1589G>A, XM_047426930.1:c.1460G>A, XM_047426932.1:c.1316G>A, XP_005245461.1:p.Gly559Asp, XP_011508144.1:p.Gly412Asp, XP_011508143.1:p.Gly468Asp, NP_067649.2:p.Gly550Asp, XP_011508141.1:p.Gly535Asp, XP_011508140.1:p.Gly535Asp, XP_011508145.1:p.Gly412Asp, XP_011508142.1:p.Gly487Asp, XP_011508148.1:p.Gly412Asp, XP_011508146.1:p.Gly343Asp, NP_001017403.1:p.Gly602Asp, XP_016857485.1:p.Gly511Asp, XP_016857486.1:p.Gly468Asp, NP_001017404.1:p.Gly463Asp, XP_047282884.1:p.Gly578Asp, XP_047282885.1:p.Gly554Asp, XP_047282887.1:p.Gly530Asp, XP_047282886.1:p.Gly487Asp, XP_047282888.1:p.Gly439Asp

                  9.

                  rs1482222390 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A,T [Show Flanks]
                    Chromosome:
                    1:202318277 (GRCh38)
                    1:202287405 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:202318276:G:A,NC_000001.11:202318276:G:T
                    Gene:
                    LGR6 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,synonymous_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000008/2 (GnomAD_exomes)
                    HGVS:
                    NC_000001.11:g.202318277G>A, NC_000001.11:g.202318277G>T, NC_000001.10:g.202287405G>A, NC_000001.10:g.202287405G>T, XM_005245404.4:c.1845G>A, XM_005245404.4:c.1845G>T, XM_005245404.3:c.1845G>A, XM_005245404.3:c.1845G>T, XM_005245404.2:c.1845G>A, XM_005245404.2:c.1845G>T, XM_005245404.1:c.1845G>A, XM_005245404.1:c.1845G>T, XM_011509842.3:c.1404G>A, XM_011509842.3:c.1404G>T, XM_011509842.2:c.1404G>A, XM_011509842.2:c.1404G>T, XM_011509842.1:c.1404G>A, XM_011509842.1:c.1404G>T, XM_011509841.3:c.1572G>A, XM_011509841.3:c.1572G>T, XM_011509841.2:c.1572G>A, XM_011509841.2:c.1572G>T, XM_011509841.1:c.1572G>A, XM_011509841.1:c.1572G>T, NM_021636.3:c.1818G>A, NM_021636.3:c.1818G>T, NM_021636.2:c.1818G>A, NM_021636.2:c.1818G>T, XM_011509839.3:c.1773G>A, XM_011509839.3:c.1773G>T, XM_011509839.2:c.1773G>A, XM_011509839.2:c.1773G>T, XM_011509839.1:c.1773G>A, XM_011509839.1:c.1773G>T, XM_011509838.3:c.1773G>A, XM_011509838.3:c.1773G>T, XM_011509838.2:c.1773G>A, XM_011509838.2:c.1773G>T, XM_011509838.1:c.1773G>A, XM_011509838.1:c.1773G>T, XM_011509843.3:c.1404G>A, XM_011509843.3:c.1404G>T, XM_011509843.2:c.1404G>A, XM_011509843.2:c.1404G>T, XM_011509843.1:c.1404G>A, XM_011509843.1:c.1404G>T, XM_011509840.3:c.1629G>A, XM_011509840.3:c.1629G>T, XM_011509840.2:c.1629G>A, XM_011509840.2:c.1629G>T, XM_011509840.1:c.1629G>A, XM_011509840.1:c.1629G>T, XM_011509846.3:c.1404G>A, XM_011509846.3:c.1404G>T, XM_011509846.2:c.1404G>A, XM_011509846.2:c.1404G>T, XM_011509846.1:c.1404G>A, XM_011509846.1:c.1404G>T, XM_011509844.3:c.1197G>A, XM_011509844.3:c.1197G>T, XM_011509844.2:c.1197G>A, XM_011509844.2:c.1197G>T, XM_011509844.1:c.1197G>A, XM_011509844.1:c.1197G>T, NM_001017403.2:c.1974G>A, NM_001017403.2:c.1974G>T, NM_001017403.1:c.1974G>A, NM_001017403.1:c.1974G>T, XM_017001996.2:c.1701G>A, XM_017001996.2:c.1701G>T, XM_017001996.1:c.1701G>A, XM_017001996.1:c.1701G>T, XM_017001997.2:c.1572G>A, XM_017001997.2:c.1572G>T, XM_017001997.1:c.1572G>A, XM_017001997.1:c.1572G>T, NM_001017404.2:c.1557G>A, NM_001017404.2:c.1557G>T, NM_001017404.1:c.1557G>A, NM_001017404.1:c.1557G>T, XM_047426928.1:c.1902G>A, XM_047426928.1:c.1902G>T, XM_047426929.1:c.1830G>A, XM_047426929.1:c.1830G>T, XM_047426931.1:c.1758G>A, XM_047426931.1:c.1758G>T, XM_047426930.1:c.1629G>A, XM_047426930.1:c.1629G>T, XM_047426932.1:c.1485G>A, XM_047426932.1:c.1485G>T

                    10.

                    rs1476601187 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>A,G [Show Flanks]
                      Chromosome:
                      1:202310210 (GRCh38)
                      1:202279338 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:202310209:C:A,NC_000001.11:202310209:C:G
                      Gene:
                      LGR6 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.0002/1 (Estonian)
                      HGVS:
                      NC_000001.11:g.202310210C>A, NC_000001.11:g.202310210C>G, NC_000001.10:g.202279338C>A, NC_000001.10:g.202279338C>G, XM_005245404.4:c.1291C>A, XM_005245404.4:c.1291C>G, XM_005245404.3:c.1291C>A, XM_005245404.3:c.1291C>G, XM_005245404.2:c.1291C>A, XM_005245404.2:c.1291C>G, XM_005245404.1:c.1291C>A, XM_005245404.1:c.1291C>G, XM_011509842.3:c.850C>A, XM_011509842.3:c.850C>G, XM_011509842.2:c.850C>A, XM_011509842.2:c.850C>G, XM_011509842.1:c.850C>A, XM_011509842.1:c.850C>G, XM_011509841.3:c.1018C>A, XM_011509841.3:c.1018C>G, XM_011509841.2:c.1018C>A, XM_011509841.2:c.1018C>G, XM_011509841.1:c.1018C>A, XM_011509841.1:c.1018C>G, NM_021636.3:c.1264C>A, NM_021636.3:c.1264C>G, NM_021636.2:c.1264C>A, NM_021636.2:c.1264C>G, XM_011509839.3:c.1219C>A, XM_011509839.3:c.1219C>G, XM_011509839.2:c.1219C>A, XM_011509839.2:c.1219C>G, XM_011509839.1:c.1219C>A, XM_011509839.1:c.1219C>G, XM_011509838.3:c.1219C>A, XM_011509838.3:c.1219C>G, XM_011509838.2:c.1219C>A, XM_011509838.2:c.1219C>G, XM_011509838.1:c.1219C>A, XM_011509838.1:c.1219C>G, XM_011509843.3:c.850C>A, XM_011509843.3:c.850C>G, XM_011509843.2:c.850C>A, XM_011509843.2:c.850C>G, XM_011509843.1:c.850C>A, XM_011509843.1:c.850C>G, XM_011509840.3:c.1075C>A, XM_011509840.3:c.1075C>G, XM_011509840.2:c.1075C>A, XM_011509840.2:c.1075C>G, XM_011509840.1:c.1075C>A, XM_011509840.1:c.1075C>G, XM_011509846.3:c.850C>A, XM_011509846.3:c.850C>G, XM_011509846.2:c.850C>A, XM_011509846.2:c.850C>G, XM_011509846.1:c.850C>A, XM_011509846.1:c.850C>G, XM_011509844.3:c.643C>A, XM_011509844.3:c.643C>G, XM_011509844.2:c.643C>A, XM_011509844.2:c.643C>G, XM_011509844.1:c.643C>A, XM_011509844.1:c.643C>G, NM_001017403.2:c.1420C>A, NM_001017403.2:c.1420C>G, NM_001017403.1:c.1420C>A, NM_001017403.1:c.1420C>G, XM_017001996.2:c.1147C>A, XM_017001996.2:c.1147C>G, XM_017001996.1:c.1147C>A, XM_017001996.1:c.1147C>G, XM_017001997.2:c.1018C>A, XM_017001997.2:c.1018C>G, XM_017001997.1:c.1018C>A, XM_017001997.1:c.1018C>G, NM_001017404.2:c.1003C>A, NM_001017404.2:c.1003C>G, NM_001017404.1:c.1003C>A, NM_001017404.1:c.1003C>G, XM_047426928.1:c.1348C>A, XM_047426928.1:c.1348C>G, XM_047426929.1:c.1276C>A, XM_047426929.1:c.1276C>G, XM_047426931.1:c.1204C>A, XM_047426931.1:c.1204C>G, XM_047426930.1:c.1075C>A, XM_047426930.1:c.1075C>G, XM_047426932.1:c.931C>A, XM_047426932.1:c.931C>G, XP_005245461.1:p.Pro431Thr, XP_005245461.1:p.Pro431Ala, XP_011508144.1:p.Pro284Thr, XP_011508144.1:p.Pro284Ala, XP_011508143.1:p.Pro340Thr, XP_011508143.1:p.Pro340Ala, NP_067649.2:p.Pro422Thr, NP_067649.2:p.Pro422Ala, XP_011508141.1:p.Pro407Thr, XP_011508141.1:p.Pro407Ala, XP_011508140.1:p.Pro407Thr, XP_011508140.1:p.Pro407Ala, XP_011508145.1:p.Pro284Thr, XP_011508145.1:p.Pro284Ala, XP_011508142.1:p.Pro359Thr, XP_011508142.1:p.Pro359Ala, XP_011508148.1:p.Pro284Thr, XP_011508148.1:p.Pro284Ala, XP_011508146.1:p.Pro215Thr, XP_011508146.1:p.Pro215Ala, NP_001017403.1:p.Pro474Thr, NP_001017403.1:p.Pro474Ala, XP_016857485.1:p.Pro383Thr, XP_016857485.1:p.Pro383Ala, XP_016857486.1:p.Pro340Thr, XP_016857486.1:p.Pro340Ala, NP_001017404.1:p.Pro335Thr, NP_001017404.1:p.Pro335Ala, XP_047282884.1:p.Pro450Thr, XP_047282884.1:p.Pro450Ala, XP_047282885.1:p.Pro426Thr, XP_047282885.1:p.Pro426Ala, XP_047282887.1:p.Pro402Thr, XP_047282887.1:p.Pro402Ala, XP_047282886.1:p.Pro359Thr, XP_047282886.1:p.Pro359Ala, XP_047282888.1:p.Pro311Thr, XP_047282888.1:p.Pro311Ala

                      11.

                      rs1475400972 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>T [Show Flanks]
                        Chromosome:
                        1:202318073 (GRCh38)
                        1:202287201 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:202318072:G:T
                        Gene:
                        LGR6 (Varview)
                        Functional Consequence:
                        synonymous_variant,coding_sequence_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000004/1 (GnomAD_exomes)
                        T=0.000004/1 (TOPMED)
                        T=0.000007/1 (GnomAD)
                        T=0.000035/1 (TOMMO)
                        HGVS:
                        NC_000001.11:g.202318073G>T, NC_000001.10:g.202287201G>T, XM_005245404.4:c.1641G>T, XM_005245404.3:c.1641G>T, XM_005245404.2:c.1641G>T, XM_005245404.1:c.1641G>T, XM_011509842.3:c.1200G>T, XM_011509842.2:c.1200G>T, XM_011509842.1:c.1200G>T, XM_011509841.3:c.1368G>T, XM_011509841.2:c.1368G>T, XM_011509841.1:c.1368G>T, NM_021636.3:c.1614G>T, NM_021636.2:c.1614G>T, XM_011509839.3:c.1569G>T, XM_011509839.2:c.1569G>T, XM_011509839.1:c.1569G>T, XM_011509838.3:c.1569G>T, XM_011509838.2:c.1569G>T, XM_011509838.1:c.1569G>T, XM_011509843.3:c.1200G>T, XM_011509843.2:c.1200G>T, XM_011509843.1:c.1200G>T, XM_011509840.3:c.1425G>T, XM_011509840.2:c.1425G>T, XM_011509840.1:c.1425G>T, XM_011509846.3:c.1200G>T, XM_011509846.2:c.1200G>T, XM_011509846.1:c.1200G>T, XM_011509844.3:c.993G>T, XM_011509844.2:c.993G>T, XM_011509844.1:c.993G>T, NM_001017403.2:c.1770G>T, NM_001017403.1:c.1770G>T, XM_017001996.2:c.1497G>T, XM_017001996.1:c.1497G>T, XM_017001997.2:c.1368G>T, XM_017001997.1:c.1368G>T, NM_001017404.2:c.1353G>T, NM_001017404.1:c.1353G>T, XM_047426928.1:c.1698G>T, XM_047426929.1:c.1626G>T, XM_047426931.1:c.1554G>T, XM_047426930.1:c.1425G>T, XM_047426932.1:c.1281G>T

                        12.

                        rs1474923986 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>G [Show Flanks]
                          Chromosome:
                          1:202214235 (GRCh38)
                          1:202183363 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:202214234:C:G
                          Gene:
                          LGR6 (Varview)
                          Functional Consequence:
                          genic_upstream_transcript_variant,coding_sequence_variant,synonymous_variant,intron_variant
                          HGVS:

                          13.

                          rs1473624419 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            1:202318084 (GRCh38)
                            1:202287212 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:202318083:T:C
                            Gene:
                            LGR6 (Varview)
                            Functional Consequence:
                            missense_variant,coding_sequence_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000008/2 (TOPMED)
                            HGVS:
                            NC_000001.11:g.202318084T>C, NC_000001.10:g.202287212T>C, XM_005245404.4:c.1652T>C, XM_005245404.3:c.1652T>C, XM_005245404.2:c.1652T>C, XM_005245404.1:c.1652T>C, XM_011509842.3:c.1211T>C, XM_011509842.2:c.1211T>C, XM_011509842.1:c.1211T>C, XM_011509841.3:c.1379T>C, XM_011509841.2:c.1379T>C, XM_011509841.1:c.1379T>C, NM_021636.3:c.1625T>C, NM_021636.2:c.1625T>C, XM_011509839.3:c.1580T>C, XM_011509839.2:c.1580T>C, XM_011509839.1:c.1580T>C, XM_011509838.3:c.1580T>C, XM_011509838.2:c.1580T>C, XM_011509838.1:c.1580T>C, XM_011509843.3:c.1211T>C, XM_011509843.2:c.1211T>C, XM_011509843.1:c.1211T>C, XM_011509840.3:c.1436T>C, XM_011509840.2:c.1436T>C, XM_011509840.1:c.1436T>C, XM_011509846.3:c.1211T>C, XM_011509846.2:c.1211T>C, XM_011509846.1:c.1211T>C, XM_011509844.3:c.1004T>C, XM_011509844.2:c.1004T>C, XM_011509844.1:c.1004T>C, NM_001017403.2:c.1781T>C, NM_001017403.1:c.1781T>C, XM_017001996.2:c.1508T>C, XM_017001996.1:c.1508T>C, XM_017001997.2:c.1379T>C, XM_017001997.1:c.1379T>C, NM_001017404.2:c.1364T>C, NM_001017404.1:c.1364T>C, XM_047426928.1:c.1709T>C, XM_047426929.1:c.1637T>C, XM_047426931.1:c.1565T>C, XM_047426930.1:c.1436T>C, XM_047426932.1:c.1292T>C, XP_005245461.1:p.Leu551Pro, XP_011508144.1:p.Leu404Pro, XP_011508143.1:p.Leu460Pro, NP_067649.2:p.Leu542Pro, XP_011508141.1:p.Leu527Pro, XP_011508140.1:p.Leu527Pro, XP_011508145.1:p.Leu404Pro, XP_011508142.1:p.Leu479Pro, XP_011508148.1:p.Leu404Pro, XP_011508146.1:p.Leu335Pro, NP_001017403.1:p.Leu594Pro, XP_016857485.1:p.Leu503Pro, XP_016857486.1:p.Leu460Pro, NP_001017404.1:p.Leu455Pro, XP_047282884.1:p.Leu570Pro, XP_047282885.1:p.Leu546Pro, XP_047282887.1:p.Leu522Pro, XP_047282886.1:p.Leu479Pro, XP_047282888.1:p.Leu431Pro

                            14.

                            rs1473128023 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>C [Show Flanks]
                              Chromosome:
                              1:202214168 (GRCh38)
                              1:202183296 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:202214167:G:C
                              Gene:
                              LGR6 (Varview)
                              Functional Consequence:
                              genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                              HGVS:

                              15.

                              rs1471415364 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                1:202301172 (GRCh38)
                                1:202270300 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:202301171:A:G
                                Gene:
                                LGR6 (Varview)
                                Functional Consequence:
                                missense_variant,coding_sequence_variant
                                Validated:
                                by frequency
                                MAF:
                                G=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000001.11:g.202301172A>G, NC_000001.10:g.202270300A>G, XM_005245404.4:c.737A>G, XM_005245404.3:c.737A>G, XM_005245404.2:c.737A>G, XM_005245404.1:c.737A>G, XM_011509842.3:c.296A>G, XM_011509842.2:c.296A>G, XM_011509842.1:c.296A>G, XM_011509841.3:c.464A>G, XM_011509841.2:c.464A>G, XM_011509841.1:c.464A>G, NM_021636.3:c.710A>G, NM_021636.2:c.710A>G, XM_011509839.3:c.737A>G, XM_011509839.2:c.737A>G, XM_011509839.1:c.737A>G, XM_011509838.3:c.665A>G, XM_011509838.2:c.665A>G, XM_011509838.1:c.665A>G, XM_011509843.3:c.296A>G, XM_011509843.2:c.296A>G, XM_011509843.1:c.296A>G, XM_011509840.3:c.521A>G, XM_011509840.2:c.521A>G, XM_011509840.1:c.521A>G, XM_011509846.3:c.296A>G, XM_011509846.2:c.296A>G, XM_011509846.1:c.296A>G, XM_011509844.3:c.89A>G, XM_011509844.2:c.89A>G, XM_011509844.1:c.89A>G, NM_001017403.2:c.866A>G, NM_001017403.1:c.866A>G, XM_017001996.2:c.737A>G, XM_017001996.1:c.737A>G, XM_017001997.2:c.464A>G, XM_017001997.1:c.464A>G, NM_001017404.2:c.449A>G, NM_001017404.1:c.449A>G, XM_047426928.1:c.866A>G, XM_047426929.1:c.866A>G, XM_047426931.1:c.650A>G, XM_047426930.1:c.665A>G, XM_047426932.1:c.449A>G, XP_005245461.1:p.Tyr246Cys, XP_011508144.1:p.Tyr99Cys, XP_011508143.1:p.Tyr155Cys, NP_067649.2:p.Tyr237Cys, XP_011508141.1:p.Tyr246Cys, XP_011508140.1:p.Tyr222Cys, XP_011508145.1:p.Tyr99Cys, XP_011508142.1:p.Tyr174Cys, XP_011508148.1:p.Tyr99Cys, XP_011508146.1:p.Tyr30Cys, NP_001017403.1:p.Tyr289Cys, XP_016857485.1:p.Tyr246Cys, XP_016857486.1:p.Tyr155Cys, NP_001017404.1:p.Tyr150Cys, XP_047282884.1:p.Tyr289Cys, XP_047282885.1:p.Tyr289Cys, XP_047282887.1:p.Tyr217Cys, XP_047282886.1:p.Tyr222Cys, XP_047282888.1:p.Tyr150Cys

                                16.

                                rs1471181006 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  1:202318759 (GRCh38)
                                  1:202287887 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:202318758:C:T
                                  Gene:
                                  LGR6 (Varview)
                                  Functional Consequence:
                                  missense_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0.000051/1 (ALFA)
                                  T=0.000004/1 (TOPMED)
                                  T=0.000008/2 (GnomAD_exomes)
                                  HGVS:
                                  NC_000001.11:g.202318759C>T, NC_000001.10:g.202287887C>T, XM_005245404.4:c.2327C>T, XM_005245404.3:c.2327C>T, XM_005245404.2:c.2327C>T, XM_005245404.1:c.2327C>T, XM_011509842.3:c.1886C>T, XM_011509842.2:c.1886C>T, XM_011509842.1:c.1886C>T, XM_011509841.3:c.2054C>T, XM_011509841.2:c.2054C>T, XM_011509841.1:c.2054C>T, NM_021636.3:c.2300C>T, NM_021636.2:c.2300C>T, XM_011509839.3:c.2255C>T, XM_011509839.2:c.2255C>T, XM_011509839.1:c.2255C>T, XM_011509838.3:c.2255C>T, XM_011509838.2:c.2255C>T, XM_011509838.1:c.2255C>T, XM_011509843.3:c.1886C>T, XM_011509843.2:c.1886C>T, XM_011509843.1:c.1886C>T, XM_011509840.3:c.2111C>T, XM_011509840.2:c.2111C>T, XM_011509840.1:c.2111C>T, XM_011509846.3:c.1886C>T, XM_011509846.2:c.1886C>T, XM_011509846.1:c.1886C>T, XM_011509844.3:c.1679C>T, XM_011509844.2:c.1679C>T, XM_011509844.1:c.1679C>T, NM_001017403.2:c.2456C>T, NM_001017403.1:c.2456C>T, XM_017001996.2:c.2183C>T, XM_017001996.1:c.2183C>T, XM_017001997.2:c.2054C>T, XM_017001997.1:c.2054C>T, NM_001017404.2:c.2039C>T, NM_001017404.1:c.2039C>T, XM_047426928.1:c.2384C>T, XM_047426929.1:c.2312C>T, XM_047426931.1:c.2240C>T, XM_047426930.1:c.2111C>T, XM_047426932.1:c.1967C>T, XP_005245461.1:p.Pro776Leu, XP_011508144.1:p.Pro629Leu, XP_011508143.1:p.Pro685Leu, NP_067649.2:p.Pro767Leu, XP_011508141.1:p.Pro752Leu, XP_011508140.1:p.Pro752Leu, XP_011508145.1:p.Pro629Leu, XP_011508142.1:p.Pro704Leu, XP_011508148.1:p.Pro629Leu, XP_011508146.1:p.Pro560Leu, NP_001017403.1:p.Pro819Leu, XP_016857485.1:p.Pro728Leu, XP_016857486.1:p.Pro685Leu, NP_001017404.1:p.Pro680Leu, XP_047282884.1:p.Pro795Leu, XP_047282885.1:p.Pro771Leu, XP_047282887.1:p.Pro747Leu, XP_047282886.1:p.Pro704Leu, XP_047282888.1:p.Pro656Leu

                                  17.

                                  rs1470496056 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    1:202276464 (GRCh38)
                                    1:202245592 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:202276463:A:G
                                    Gene:
                                    LGR6 (Varview)
                                    Functional Consequence:
                                    genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                                    HGVS:
                                    NC_000001.11:g.202276464A>G, NC_000001.10:g.202245592A>G, XM_005245404.4:c.458A>G, XM_005245404.3:c.458A>G, XM_005245404.2:c.458A>G, XM_005245404.1:c.458A>G, XM_011509842.3:c.17A>G, XM_011509842.2:c.17A>G, XM_011509842.1:c.17A>G, XM_011509841.3:c.185A>G, XM_011509841.2:c.185A>G, XM_011509841.1:c.185A>G, NM_021636.3:c.431A>G, NM_021636.2:c.431A>G, XM_011509839.3:c.458A>G, XM_011509839.2:c.458A>G, XM_011509839.1:c.458A>G, XM_011509838.3:c.458A>G, XM_011509838.2:c.458A>G, XM_011509838.1:c.458A>G, XM_011509843.3:c.17A>G, XM_011509843.2:c.17A>G, XM_011509843.1:c.17A>G, XM_011509846.3:c.17A>G, XM_011509846.2:c.17A>G, XM_011509846.1:c.17A>G, NM_001017403.2:c.587A>G, NM_001017403.1:c.587A>G, XM_017001996.2:c.458A>G, XM_017001996.1:c.458A>G, XM_017001997.2:c.185A>G, XM_017001997.1:c.185A>G, XM_047426928.1:c.587A>G, XM_047426929.1:c.587A>G, XM_047426930.1:c.458A>G, XP_005245461.1:p.Asn153Ser, XP_011508144.1:p.Asn6Ser, XP_011508143.1:p.Asn62Ser, NP_067649.2:p.Asn144Ser, XP_011508141.1:p.Asn153Ser, XP_011508140.1:p.Asn153Ser, XP_011508145.1:p.Asn6Ser, XP_011508148.1:p.Asn6Ser, NP_001017403.1:p.Asn196Ser, XP_016857485.1:p.Asn153Ser, XP_016857486.1:p.Asn62Ser, XP_047282884.1:p.Asn196Ser, XP_047282885.1:p.Asn196Ser, XP_047282886.1:p.Asn153Ser

                                    18.

                                    rs1468844419 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      1:202310257 (GRCh38)
                                      1:202279385 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:202310256:C:T
                                      Gene:
                                      LGR6 (Varview)
                                      Functional Consequence:
                                      synonymous_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      T=0.000031/1 (ALFA)
                                      T=0.000004/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000001.11:g.202310257C>T, NC_000001.10:g.202279385C>T, XM_005245404.4:c.1338C>T, XM_005245404.3:c.1338C>T, XM_005245404.2:c.1338C>T, XM_005245404.1:c.1338C>T, XM_011509842.3:c.897C>T, XM_011509842.2:c.897C>T, XM_011509842.1:c.897C>T, XM_011509841.3:c.1065C>T, XM_011509841.2:c.1065C>T, XM_011509841.1:c.1065C>T, NM_021636.3:c.1311C>T, NM_021636.2:c.1311C>T, XM_011509839.3:c.1266C>T, XM_011509839.2:c.1266C>T, XM_011509839.1:c.1266C>T, XM_011509838.3:c.1266C>T, XM_011509838.2:c.1266C>T, XM_011509838.1:c.1266C>T, XM_011509843.3:c.897C>T, XM_011509843.2:c.897C>T, XM_011509843.1:c.897C>T, XM_011509840.3:c.1122C>T, XM_011509840.2:c.1122C>T, XM_011509840.1:c.1122C>T, XM_011509846.3:c.897C>T, XM_011509846.2:c.897C>T, XM_011509846.1:c.897C>T, XM_011509844.3:c.690C>T, XM_011509844.2:c.690C>T, XM_011509844.1:c.690C>T, NM_001017403.2:c.1467C>T, NM_001017403.1:c.1467C>T, XM_017001996.2:c.1194C>T, XM_017001996.1:c.1194C>T, XM_017001997.2:c.1065C>T, XM_017001997.1:c.1065C>T, NM_001017404.2:c.1050C>T, NM_001017404.1:c.1050C>T, XM_047426928.1:c.1395C>T, XM_047426929.1:c.1323C>T, XM_047426931.1:c.1251C>T, XM_047426930.1:c.1122C>T, XM_047426932.1:c.978C>T

                                      19.

                                      rs1466334254 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>A [Show Flanks]
                                        Chromosome:
                                        1:202214224 (GRCh38)
                                        1:202183352 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:202214223:C:A
                                        Gene:
                                        LGR6 (Varview)
                                        Functional Consequence:
                                        genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                                        HGVS:

                                        20.

                                        rs1465156122 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>A [Show Flanks]
                                          Chromosome:
                                          1:202318965 (GRCh38)
                                          1:202288093 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:202318964:C:A
                                          Gene:
                                          LGR6 (Varview)
                                          Functional Consequence:
                                          missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          A=0.000008/2 (GnomAD_exomes)
                                          HGVS:
                                          NC_000001.11:g.202318965C>A, NC_000001.10:g.202288093C>A, XM_005245404.4:c.2533C>A, XM_005245404.3:c.2533C>A, XM_005245404.2:c.2533C>A, XM_005245404.1:c.2533C>A, XM_011509842.3:c.2092C>A, XM_011509842.2:c.2092C>A, XM_011509842.1:c.2092C>A, XM_011509841.3:c.2260C>A, XM_011509841.2:c.2260C>A, XM_011509841.1:c.2260C>A, NM_021636.3:c.2506C>A, NM_021636.2:c.2506C>A, XM_011509839.3:c.2461C>A, XM_011509839.2:c.2461C>A, XM_011509839.1:c.2461C>A, XM_011509838.3:c.2461C>A, XM_011509838.2:c.2461C>A, XM_011509838.1:c.2461C>A, XM_011509843.3:c.2092C>A, XM_011509843.2:c.2092C>A, XM_011509843.1:c.2092C>A, XM_011509840.3:c.2317C>A, XM_011509840.2:c.2317C>A, XM_011509840.1:c.2317C>A, XM_011509846.3:c.2092C>A, XM_011509846.2:c.2092C>A, XM_011509846.1:c.2092C>A, XM_011509844.3:c.1885C>A, XM_011509844.2:c.1885C>A, XM_011509844.1:c.1885C>A, NM_001017403.2:c.2662C>A, NM_001017403.1:c.2662C>A, XM_017001996.2:c.2389C>A, XM_017001996.1:c.2389C>A, XM_017001997.2:c.2260C>A, XM_017001997.1:c.2260C>A, NM_001017404.2:c.2245C>A, NM_001017404.1:c.2245C>A, XM_047426928.1:c.2590C>A, XM_047426929.1:c.2518C>A, XM_047426931.1:c.2446C>A, XM_047426930.1:c.2317C>A, XM_047426932.1:c.2173C>A, XP_005245461.1:p.Pro845Thr, XP_011508144.1:p.Pro698Thr, XP_011508143.1:p.Pro754Thr, NP_067649.2:p.Pro836Thr, XP_011508141.1:p.Pro821Thr, XP_011508140.1:p.Pro821Thr, XP_011508145.1:p.Pro698Thr, XP_011508142.1:p.Pro773Thr, XP_011508148.1:p.Pro698Thr, XP_011508146.1:p.Pro629Thr, NP_001017403.1:p.Pro888Thr, XP_016857485.1:p.Pro797Thr, XP_016857486.1:p.Pro754Thr, NP_001017404.1:p.Pro749Thr, XP_047282884.1:p.Pro864Thr, XP_047282885.1:p.Pro840Thr, XP_047282887.1:p.Pro816Thr, XP_047282886.1:p.Pro773Thr, XP_047282888.1:p.Pro725Thr

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