U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Protein

Items: 1 to 20 of 409

1.

rs1488630799 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    19:54193197 (GRCh38)
    19:54697052 (GRCh37)
    Canonical SPDI:
    NC_000019.10:54193196:C:T
    Gene:
    TSEN34 (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    Validated:
    by frequency
    MAF:
    T=0.000004/1 (GnomAD_exomes)
    HGVS:

    2.

    rs1487480047 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G [Show Flanks]
      Chromosome:
      19:54191392 (GRCh38)
      19:54695243 (GRCh37)
      Canonical SPDI:
      NC_000019.10:54191391:C:G
      Gene:
      TSEN34 (Varview), MBOAT7 (Varview)
      Functional Consequence:
      2KB_upstream_variant,missense_variant,upstream_transcript_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa
      MAF:
      G=0.000071/1 (ALFA)
      G=0.000004/1 (TOPMED)
      HGVS:
      NC_000019.10:g.54191392C>G, NW_004166865.1:g.165759C>G, NG_033045.2:g.3484G>C, NM_024075.5:c.28C>G, NM_024075.4:c.28C>G, NM_024075.3:c.28C>G, NM_001077446.4:c.28C>G, NM_001077446.3:c.28C>G, NM_001077446.2:c.28C>G, NM_001282332.2:c.28C>G, NM_001282332.1:c.28C>G, NM_001282333.2:c.28C>G, NM_001282333.1:c.37C>G, NM_001386740.1:c.28C>G, NG_015810.2:g.6158C>G, NW_003571061.2:g.166357C>G, NW_003571059.2:g.166357C>G, NW_003571058.2:g.166357C>G, NW_003571057.2:g.166357C>G, NW_003571056.2:g.166357C>G, NW_003571055.2:g.166357C>G, NW_003571061.1:g.166356C>G, NW_003571060.1:g.166356C>G, NW_003571054.1:g.166189C>G, NT_187693.1:g.166357C>G, NC_000019.9:g.54695243C>G, XM_011527294.4:c.28C>G, XM_011527294.3:c.28C>G, XM_011527294.2:c.28C>G, XM_011527294.1:c.28C>G, XM_047439391.1:c.28C>G, NP_076980.2:p.Arg10Gly, NP_001070914.1:p.Arg10Gly, NP_001269261.1:p.Arg10Gly, NP_001269262.2:p.Arg10Gly, NP_001373669.1:p.Arg10Gly, XP_011525596.1:p.Arg10Gly, XP_047295347.1:p.Arg10Gly

      3.

      rs1483718236 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        19:54193202 (GRCh38)
        19:54697057 (GRCh37)
        Canonical SPDI:
        NC_000019.10:54193201:A:G
        Gene:
        TSEN34 (Varview)
        Functional Consequence:
        missense_variant,coding_sequence_variant
        Validated:
        by frequency
        MAF:
        G=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000019.10:g.54193202A>G, NW_004166865.1:g.167569A>G, NG_033045.2:g.1674T>C, NM_024075.5:c.773A>G, NM_024075.4:c.773A>G, NM_024075.3:c.773A>G, NM_001077446.4:c.773A>G, NM_001077446.3:c.773A>G, NM_001077446.2:c.773A>G, NM_001282332.2:c.773A>G, NM_001282332.1:c.773A>G, NM_001282333.2:c.773A>G, NM_001282333.1:c.782A>G, NM_001386740.1:c.773A>G, NG_015810.2:g.7968A>G, NW_003571061.2:g.168171A>G, NW_003571059.2:g.168171A>G, NW_003571058.2:g.168171A>G, NW_003571057.2:g.168171A>G, NW_003571056.2:g.168171A>G, NW_003571055.2:g.168171A>G, NW_003571061.1:g.168170A>G, NW_003571060.1:g.168165A>G, NW_003571054.1:g.167998A>G, NT_187693.1:g.168171A>G, NC_000019.9:g.54697057A>G, XM_011527294.4:c.773A>G, XM_011527294.3:c.773A>G, XM_011527294.2:c.773A>G, XM_011527294.1:c.773A>G, XM_047439391.1:c.773A>G, NP_076980.2:p.Tyr258Cys, NP_001070914.1:p.Tyr258Cys, NP_001269261.1:p.Tyr258Cys, NP_001269262.2:p.Tyr258Cys, NP_001373669.1:p.Tyr258Cys, XP_011525596.1:p.Tyr258Cys, XP_047295347.1:p.Tyr258Cys

        4.

        rs1482935701 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,T [Show Flanks]
          Chromosome:
          19:54191575 (GRCh38)
          19:54695426 (GRCh37)
          Canonical SPDI:
          NC_000019.10:54191574:G:A,NC_000019.10:54191574:G:T
          Gene:
          TSEN34 (Varview), MBOAT7 (Varview)
          Functional Consequence:
          2KB_upstream_variant,missense_variant,upstream_transcript_variant,coding_sequence_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000019/5 (TOPMED)
          T=0.000021/3 (GnomAD)
          HGVS:
          NC_000019.10:g.54191575G>A, NC_000019.10:g.54191575G>T, NW_004166865.1:g.165942G>A, NW_004166865.1:g.165942G>T, NG_033045.2:g.3301C>T, NG_033045.2:g.3301C>A, NM_024075.5:c.211G>A, NM_024075.5:c.211G>T, NM_024075.4:c.211G>A, NM_024075.4:c.211G>T, NM_024075.3:c.211G>A, NM_024075.3:c.211G>T, NM_001077446.4:c.211G>A, NM_001077446.4:c.211G>T, NM_001077446.3:c.211G>A, NM_001077446.3:c.211G>T, NM_001077446.2:c.211G>A, NM_001077446.2:c.211G>T, NM_001282332.2:c.211G>A, NM_001282332.2:c.211G>T, NM_001282332.1:c.211G>A, NM_001282332.1:c.211G>T, NM_001282333.2:c.211G>A, NM_001282333.2:c.211G>T, NM_001282333.1:c.220G>A, NM_001282333.1:c.220G>T, NM_001386740.1:c.211G>A, NM_001386740.1:c.211G>T, NG_015810.2:g.6341G>A, NG_015810.2:g.6341G>T, NW_003571061.2:g.166540G>A, NW_003571061.2:g.166540G>T, NW_003571059.2:g.166540G>A, NW_003571059.2:g.166540G>T, NW_003571058.2:g.166540G>A, NW_003571058.2:g.166540G>T, NW_003571057.2:g.166540G>A, NW_003571057.2:g.166540G>T, NW_003571056.2:g.166540G>A, NW_003571056.2:g.166540G>T, NW_003571055.2:g.166540G>A, NW_003571055.2:g.166540G>T, NW_003571061.1:g.166539G>A, NW_003571061.1:g.166539G>T, NW_003571060.1:g.166539G>A, NW_003571060.1:g.166539G>T, NW_003571054.1:g.166372G>A, NW_003571054.1:g.166372G>T, NT_187693.1:g.166540G>A, NT_187693.1:g.166540G>T, NC_000019.9:g.54695426G>A, NC_000019.9:g.54695426G>T, XM_011527294.4:c.211G>A, XM_011527294.4:c.211G>T, XM_011527294.3:c.211G>A, XM_011527294.3:c.211G>T, XM_011527294.2:c.211G>A, XM_011527294.2:c.211G>T, XM_011527294.1:c.211G>A, XM_011527294.1:c.211G>T, XM_047439391.1:c.211G>A, XM_047439391.1:c.211G>T, NP_076980.2:p.Ala71Thr, NP_076980.2:p.Ala71Ser, NP_001070914.1:p.Ala71Thr, NP_001070914.1:p.Ala71Ser, NP_001269261.1:p.Ala71Thr, NP_001269261.1:p.Ala71Ser, NP_001269262.2:p.Ala71Thr, NP_001269262.2:p.Ala71Ser, NP_001373669.1:p.Ala71Thr, NP_001373669.1:p.Ala71Ser, XP_011525596.1:p.Ala71Thr, XP_011525596.1:p.Ala71Ser, XP_047295347.1:p.Ala71Thr, XP_047295347.1:p.Ala71Ser

          5.

          rs1482713429 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            19:54192135 (GRCh38)
            19:54695986 (GRCh37)
            Canonical SPDI:
            NC_000019.10:54192134:A:G
            Gene:
            TSEN34 (Varview)
            Functional Consequence:
            synonymous_variant,coding_sequence_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            G=0.000007/1 (GnomAD)
            HGVS:

            6.

            rs1481901431 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>C [Show Flanks]
              Chromosome:
              19:54191491 (GRCh38)
              19:54695342 (GRCh37)
              Canonical SPDI:
              NC_000019.10:54191490:A:C
              Gene:
              TSEN34 (Varview), MBOAT7 (Varview)
              Functional Consequence:
              2KB_upstream_variant,missense_variant,upstream_transcript_variant,coding_sequence_variant
              Validated:
              by frequency
              MAF:
              C=0.000006/1 (GnomAD_exomes)
              HGVS:
              NC_000019.10:g.54191491A>C, NW_004166865.1:g.165858A>C, NG_033045.2:g.3385T>G, NM_024075.5:c.127A>C, NM_024075.4:c.127A>C, NM_024075.3:c.127A>C, NM_001077446.4:c.127A>C, NM_001077446.3:c.127A>C, NM_001077446.2:c.127A>C, NM_001282332.2:c.127A>C, NM_001282332.1:c.127A>C, NM_001282333.2:c.127A>C, NM_001282333.1:c.136A>C, NM_001386740.1:c.127A>C, NG_015810.2:g.6257A>C, NW_003571061.2:g.166456A>C, NW_003571059.2:g.166456A>C, NW_003571058.2:g.166456A>C, NW_003571057.2:g.166456A>C, NW_003571056.2:g.166456A>C, NW_003571055.2:g.166456A>C, NW_003571061.1:g.166455A>C, NW_003571060.1:g.166455A>C, NW_003571054.1:g.166288A>C, NT_187693.1:g.166456A>C, NC_000019.9:g.54695342A>C, XM_011527294.4:c.127A>C, XM_011527294.3:c.127A>C, XM_011527294.2:c.127A>C, XM_011527294.1:c.127A>C, XM_047439391.1:c.127A>C, NP_076980.2:p.Asn43His, NP_001070914.1:p.Asn43His, NP_001269261.1:p.Asn43His, NP_001269262.2:p.Asn43His, NP_001373669.1:p.Asn43His, XP_011525596.1:p.Asn43His, XP_047295347.1:p.Asn43His

              7.

              rs1481439511 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                19:54191916 (GRCh38)
                19:54695767 (GRCh37)
                Canonical SPDI:
                NC_000019.10:54191915:G:A
                Gene:
                TSEN34 (Varview)
                Functional Consequence:
                missense_variant,coding_sequence_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0.000031/1 (ALFA)
                A=0.000004/1 (TOPMED)
                A=0.000008/2 (GnomAD_exomes)
                A=0.000014/2 (GnomAD)
                HGVS:
                NC_000019.10:g.54191916G>A, NW_004166865.1:g.166283G>A, NG_033045.2:g.2960C>T, NM_024075.5:c.439G>A, NM_024075.4:c.439G>A, NM_024075.3:c.439G>A, NM_001077446.4:c.439G>A, NM_001077446.3:c.439G>A, NM_001077446.2:c.439G>A, NM_001282332.2:c.439G>A, NM_001282332.1:c.439G>A, NM_001282333.2:c.439G>A, NM_001282333.1:c.448G>A, NM_001386740.1:c.439G>A, NG_015810.2:g.6682G>A, NW_003571061.2:g.166881G>A, NW_003571059.2:g.166881G>A, NW_003571058.2:g.166881G>A, NW_003571057.2:g.166881G>A, NW_003571056.2:g.166881G>A, NW_003571055.2:g.166881G>A, NW_003571061.1:g.166880G>A, NW_003571060.1:g.166880G>A, NW_003571054.1:g.166713G>A, NT_187693.1:g.166881G>A, NC_000019.9:g.54695767G>A, XM_011527294.4:c.439G>A, XM_011527294.3:c.439G>A, XM_011527294.2:c.439G>A, XM_011527294.1:c.439G>A, XM_047439391.1:c.439G>A, NP_076980.2:p.Glu147Lys, NP_001070914.1:p.Glu147Lys, NP_001269261.1:p.Glu147Lys, NP_001269262.2:p.Glu147Lys, NP_001373669.1:p.Glu147Lys, XP_011525596.1:p.Glu147Lys, XP_047295347.1:p.Glu147Lys

                8.

                rs1474571766 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>A,G [Show Flanks]
                  Chromosome:
                  19:54191495 (GRCh38)
                  19:54695346 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:54191494:C:A,NC_000019.10:54191494:C:G
                  Gene:
                  TSEN34 (Varview), MBOAT7 (Varview)
                  Functional Consequence:
                  2KB_upstream_variant,missense_variant,coding_sequence_variant,stop_gained,upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0.000059/1 (ALFA)
                  G=0.000012/2 (GnomAD_exomes)
                  G=0.000021/3 (GnomAD)
                  G=0.000026/7 (TOPMED)
                  G=0.000035/1 (TOMMO)
                  HGVS:
                  NC_000019.10:g.54191495C>A, NC_000019.10:g.54191495C>G, NW_004166865.1:g.165862C>A, NW_004166865.1:g.165862C>G, NG_033045.2:g.3381G>T, NG_033045.2:g.3381G>C, NM_024075.5:c.131C>A, NM_024075.5:c.131C>G, NM_024075.4:c.131C>A, NM_024075.4:c.131C>G, NM_024075.3:c.131C>A, NM_024075.3:c.131C>G, NM_001077446.4:c.131C>A, NM_001077446.4:c.131C>G, NM_001077446.3:c.131C>A, NM_001077446.3:c.131C>G, NM_001077446.2:c.131C>A, NM_001077446.2:c.131C>G, NM_001282332.2:c.131C>A, NM_001282332.2:c.131C>G, NM_001282332.1:c.131C>A, NM_001282332.1:c.131C>G, NM_001282333.2:c.131C>A, NM_001282333.2:c.131C>G, NM_001282333.1:c.140C>A, NM_001282333.1:c.140C>G, NM_001386740.1:c.131C>A, NM_001386740.1:c.131C>G, NG_015810.2:g.6261C>A, NG_015810.2:g.6261C>G, NW_003571061.2:g.166460C>A, NW_003571061.2:g.166460C>G, NW_003571059.2:g.166460C>A, NW_003571059.2:g.166460C>G, NW_003571058.2:g.166460C>A, NW_003571058.2:g.166460C>G, NW_003571057.2:g.166460C>A, NW_003571057.2:g.166460C>G, NW_003571056.2:g.166460C>A, NW_003571056.2:g.166460C>G, NW_003571055.2:g.166460C>A, NW_003571055.2:g.166460C>G, NW_003571061.1:g.166459C>A, NW_003571061.1:g.166459C>G, NW_003571060.1:g.166459C>A, NW_003571060.1:g.166459C>G, NW_003571054.1:g.166292C>A, NW_003571054.1:g.166292C>G, NT_187693.1:g.166460C>A, NT_187693.1:g.166460C>G, NC_000019.9:g.54695346C>A, NC_000019.9:g.54695346C>G, XM_011527294.4:c.131C>A, XM_011527294.4:c.131C>G, XM_011527294.3:c.131C>A, XM_011527294.3:c.131C>G, XM_011527294.2:c.131C>A, XM_011527294.2:c.131C>G, XM_011527294.1:c.131C>A, XM_011527294.1:c.131C>G, XM_047439391.1:c.131C>A, XM_047439391.1:c.131C>G, NP_076980.2:p.Ser44Ter, NP_076980.2:p.Ser44Trp, NP_001070914.1:p.Ser44Ter, NP_001070914.1:p.Ser44Trp, NP_001269261.1:p.Ser44Ter, NP_001269261.1:p.Ser44Trp, NP_001269262.2:p.Ser44Ter, NP_001269262.2:p.Ser44Trp, NP_001373669.1:p.Ser44Ter, NP_001373669.1:p.Ser44Trp, XP_011525596.1:p.Ser44Ter, XP_011525596.1:p.Ser44Trp, XP_047295347.1:p.Ser44Ter, XP_047295347.1:p.Ser44Trp

                  9.

                  rs1471434668 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    19:54191846 (GRCh38)
                    19:54695697 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:54191845:G:A
                    Gene:
                    TSEN34 (Varview)
                    Functional Consequence:
                    synonymous_variant,coding_sequence_variant
                    Clinical significance:
                    uncertain-significance
                    Validated:
                    by frequency,by alfa
                    MAF:
                    A=0./0 (ALFA)
                    A=0.000008/2 (TOPMED)
                    HGVS:

                    10.

                    rs1463790091 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,C [Show Flanks]
                      Chromosome:
                      19:54192149 (GRCh38)
                      19:54696000 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:54192148:G:A,NC_000019.10:54192148:G:C
                      Gene:
                      TSEN34 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      C=0./0 (ALFA)
                      C=0.000004/1 (GnomAD_exomes)
                      C=0.000019/5 (TOPMED)
                      C=0.000036/5 (GnomAD)
                      HGVS:
                      NC_000019.10:g.54192149G>A, NC_000019.10:g.54192149G>C, NW_004166865.1:g.166516G>A, NW_004166865.1:g.166516G>C, NG_033045.2:g.2727C>T, NG_033045.2:g.2727C>G, NM_024075.5:c.521G>A, NM_024075.5:c.521G>C, NM_024075.4:c.521G>A, NM_024075.4:c.521G>C, NM_024075.3:c.521G>A, NM_024075.3:c.521G>C, NM_001077446.4:c.521G>A, NM_001077446.4:c.521G>C, NM_001077446.3:c.521G>A, NM_001077446.3:c.521G>C, NM_001077446.2:c.521G>A, NM_001077446.2:c.521G>C, NM_001282332.2:c.521G>A, NM_001282332.2:c.521G>C, NM_001282332.1:c.521G>A, NM_001282332.1:c.521G>C, NM_001282333.2:c.521G>A, NM_001282333.2:c.521G>C, NM_001282333.1:c.530G>A, NM_001282333.1:c.530G>C, NM_001386740.1:c.521G>A, NM_001386740.1:c.521G>C, NG_015810.2:g.6915G>A, NG_015810.2:g.6915G>C, NW_003571061.2:g.167114G>A, NW_003571061.2:g.167114G>C, NW_003571059.2:g.167114G>A, NW_003571059.2:g.167114G>C, NW_003571058.2:g.167114G>A, NW_003571058.2:g.167114G>C, NW_003571057.2:g.167114G>A, NW_003571057.2:g.167114G>C, NW_003571056.2:g.167114G>A, NW_003571056.2:g.167114G>C, NW_003571055.2:g.167114G>A, NW_003571055.2:g.167114G>C, NW_003571061.1:g.167113G>A, NW_003571061.1:g.167113G>C, NW_003571060.1:g.167113G>A, NW_003571060.1:g.167113G>C, NW_003571054.1:g.166946G>A, NW_003571054.1:g.166946G>C, NT_187693.1:g.167114G>A, NT_187693.1:g.167114G>C, NC_000019.9:g.54696000G>A, NC_000019.9:g.54696000G>C, XM_011527294.4:c.521G>A, XM_011527294.4:c.521G>C, XM_011527294.3:c.521G>A, XM_011527294.3:c.521G>C, XM_011527294.2:c.521G>A, XM_011527294.2:c.521G>C, XM_011527294.1:c.521G>A, XM_011527294.1:c.521G>C, XM_047439391.1:c.521G>A, XM_047439391.1:c.521G>C, NP_076980.2:p.Gly174Glu, NP_076980.2:p.Gly174Ala, NP_001070914.1:p.Gly174Glu, NP_001070914.1:p.Gly174Ala, NP_001269261.1:p.Gly174Glu, NP_001269261.1:p.Gly174Ala, NP_001269262.2:p.Gly174Glu, NP_001269262.2:p.Gly174Ala, NP_001373669.1:p.Gly174Glu, NP_001373669.1:p.Gly174Ala, XP_011525596.1:p.Gly174Glu, XP_011525596.1:p.Gly174Ala, XP_047295347.1:p.Gly174Glu, XP_047295347.1:p.Gly174Ala

                      11.

                      rs1463298158 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>G,T [Show Flanks]
                        Chromosome:
                        19:54191862 (GRCh38)
                        19:54695713 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:54191861:C:G,NC_000019.10:54191861:C:T
                        Gene:
                        TSEN34 (Varview)
                        Functional Consequence:
                        stop_gained,coding_sequence_variant,missense_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        HGVS:
                        NC_000019.10:g.54191862C>G, NC_000019.10:g.54191862C>T, NW_004166865.1:g.166229C>G, NW_004166865.1:g.166229C>T, NG_033045.2:g.3014G>C, NG_033045.2:g.3014G>A, NM_024075.5:c.385C>G, NM_024075.5:c.385C>T, NM_024075.4:c.385C>G, NM_024075.4:c.385C>T, NM_024075.3:c.385C>G, NM_024075.3:c.385C>T, NM_001077446.4:c.385C>G, NM_001077446.4:c.385C>T, NM_001077446.3:c.385C>G, NM_001077446.3:c.385C>T, NM_001077446.2:c.385C>G, NM_001077446.2:c.385C>T, NM_001282332.2:c.385C>G, NM_001282332.2:c.385C>T, NM_001282332.1:c.385C>G, NM_001282332.1:c.385C>T, NM_001282333.2:c.385C>G, NM_001282333.2:c.385C>T, NM_001282333.1:c.394C>G, NM_001282333.1:c.394C>T, NM_001386740.1:c.385C>G, NM_001386740.1:c.385C>T, NG_015810.2:g.6628C>G, NG_015810.2:g.6628C>T, NW_003571061.2:g.166827C>G, NW_003571061.2:g.166827C>T, NW_003571059.2:g.166827C>G, NW_003571059.2:g.166827C>T, NW_003571058.2:g.166827C>G, NW_003571058.2:g.166827C>T, NW_003571057.2:g.166827C>G, NW_003571057.2:g.166827C>T, NW_003571056.2:g.166827C>G, NW_003571056.2:g.166827C>T, NW_003571055.2:g.166827C>G, NW_003571055.2:g.166827C>T, NW_003571061.1:g.166826C>G, NW_003571061.1:g.166826C>T, NW_003571060.1:g.166826C>G, NW_003571060.1:g.166826C>T, NW_003571054.1:g.166659C>G, NW_003571054.1:g.166659C>T, NT_187693.1:g.166827C>G, NT_187693.1:g.166827C>T, NC_000019.9:g.54695713C>G, NC_000019.9:g.54695713C>T, XM_011527294.4:c.385C>G, XM_011527294.4:c.385C>T, XM_011527294.3:c.385C>G, XM_011527294.3:c.385C>T, XM_011527294.2:c.385C>G, XM_011527294.2:c.385C>T, XM_011527294.1:c.385C>G, XM_011527294.1:c.385C>T, XM_047439391.1:c.385C>G, XM_047439391.1:c.385C>T, NP_076980.2:p.Gln129Glu, NP_076980.2:p.Gln129Ter, NP_001070914.1:p.Gln129Glu, NP_001070914.1:p.Gln129Ter, NP_001269261.1:p.Gln129Glu, NP_001269261.1:p.Gln129Ter, NP_001269262.2:p.Gln129Glu, NP_001269262.2:p.Gln129Ter, NP_001373669.1:p.Gln129Glu, NP_001373669.1:p.Gln129Ter, XP_011525596.1:p.Gln129Glu, XP_011525596.1:p.Gln129Ter, XP_047295347.1:p.Gln129Glu, XP_047295347.1:p.Gln129Ter

                        12.

                        rs1462473161 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          A>G,T [Show Flanks]
                          Chromosome:
                          19:54191463 (GRCh38)
                          19:54695314 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:54191462:A:G,NC_000019.10:54191462:A:T
                          Gene:
                          TSEN34 (Varview), MBOAT7 (Varview)
                          Functional Consequence:
                          2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant,synonymous_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          G=0.000021/3 (GnomAD_exomes)
                          HGVS:
                          NC_000019.10:g.54191463A>G, NC_000019.10:g.54191463A>T, NW_004166865.1:g.165830A>G, NW_004166865.1:g.165830A>T, NG_033045.2:g.3413T>C, NG_033045.2:g.3413T>A, NM_024075.5:c.99A>G, NM_024075.5:c.99A>T, NM_024075.4:c.99A>G, NM_024075.4:c.99A>T, NM_024075.3:c.99A>G, NM_024075.3:c.99A>T, NM_001077446.4:c.99A>G, NM_001077446.4:c.99A>T, NM_001077446.3:c.99A>G, NM_001077446.3:c.99A>T, NM_001077446.2:c.99A>G, NM_001077446.2:c.99A>T, NM_001282332.2:c.99A>G, NM_001282332.2:c.99A>T, NM_001282332.1:c.99A>G, NM_001282332.1:c.99A>T, NM_001282333.2:c.99A>G, NM_001282333.2:c.99A>T, NM_001282333.1:c.108A>G, NM_001282333.1:c.108A>T, NM_001386740.1:c.99A>G, NM_001386740.1:c.99A>T, NG_015810.2:g.6229A>G, NG_015810.2:g.6229A>T, NW_003571061.2:g.166428A>G, NW_003571061.2:g.166428A>T, NW_003571059.2:g.166428A>G, NW_003571059.2:g.166428A>T, NW_003571058.2:g.166428A>G, NW_003571058.2:g.166428A>T, NW_003571057.2:g.166428A>G, NW_003571057.2:g.166428A>T, NW_003571056.2:g.166428A>G, NW_003571056.2:g.166428A>T, NW_003571055.2:g.166428A>G, NW_003571055.2:g.166428A>T, NW_003571061.1:g.166427A>G, NW_003571061.1:g.166427A>T, NW_003571060.1:g.166427A>G, NW_003571060.1:g.166427A>T, NW_003571054.1:g.166260A>G, NW_003571054.1:g.166260A>T, NT_187693.1:g.166428A>G, NT_187693.1:g.166428A>T, NC_000019.9:g.54695314A>G, NC_000019.9:g.54695314A>T, XM_011527294.4:c.99A>G, XM_011527294.4:c.99A>T, XM_011527294.3:c.99A>G, XM_011527294.3:c.99A>T, XM_011527294.2:c.99A>G, XM_011527294.2:c.99A>T, XM_011527294.1:c.99A>G, XM_011527294.1:c.99A>T, XM_047439391.1:c.99A>G, XM_047439391.1:c.99A>T

                          13.

                          rs1461253754 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            A>T [Show Flanks]
                            Chromosome:
                            19:54191877 (GRCh38)
                            19:54695728 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:54191876:A:T
                            Gene:
                            TSEN34 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,missense_variant
                            HGVS:
                            NC_000019.10:g.54191877A>T, NW_004166865.1:g.166244A>T, NG_033045.2:g.2999T>A, NM_024075.5:c.400A>T, NM_024075.4:c.400A>T, NM_024075.3:c.400A>T, NM_001077446.4:c.400A>T, NM_001077446.3:c.400A>T, NM_001077446.2:c.400A>T, NM_001282332.2:c.400A>T, NM_001282332.1:c.400A>T, NM_001282333.2:c.400A>T, NM_001282333.1:c.409A>T, NM_001386740.1:c.400A>T, NG_015810.2:g.6643A>T, NW_003571061.2:g.166842A>T, NW_003571059.2:g.166842A>T, NW_003571058.2:g.166842A>T, NW_003571057.2:g.166842A>T, NW_003571056.2:g.166842A>T, NW_003571055.2:g.166842A>T, NW_003571061.1:g.166841A>T, NW_003571060.1:g.166841A>T, NW_003571054.1:g.166674A>T, NT_187693.1:g.166842A>T, NC_000019.9:g.54695728A>T, XM_011527294.4:c.400A>T, XM_011527294.3:c.400A>T, XM_011527294.2:c.400A>T, XM_011527294.1:c.400A>T, XM_047439391.1:c.400A>T, NP_076980.2:p.Ser134Cys, NP_001070914.1:p.Ser134Cys, NP_001269261.1:p.Ser134Cys, NP_001269262.2:p.Ser134Cys, NP_001373669.1:p.Ser134Cys, XP_011525596.1:p.Ser134Cys, XP_047295347.1:p.Ser134Cys

                            14.

                            rs1459924515 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A,T [Show Flanks]
                              Chromosome:
                              19:54192349 (GRCh38)
                              19:54696200 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:54192348:G:A,NC_000019.10:54192348:G:T
                              Gene:
                              TSEN34 (Varview)
                              Functional Consequence:
                              stop_gained,coding_sequence_variant,missense_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0./0 (ALFA)
                              A=0.000004/1 (GnomAD_exomes)
                              T=0.000004/1 (TOPMED)
                              T=0.000007/1 (GnomAD)
                              HGVS:
                              NC_000019.10:g.54192349G>A, NC_000019.10:g.54192349G>T, NW_004166865.1:g.166716G>A, NW_004166865.1:g.166716G>T, NG_033045.2:g.2527C>T, NG_033045.2:g.2527C>A, NM_024075.5:c.721G>A, NM_024075.5:c.721G>T, NM_024075.4:c.721G>A, NM_024075.4:c.721G>T, NM_024075.3:c.721G>A, NM_024075.3:c.721G>T, NM_001077446.4:c.721G>A, NM_001077446.4:c.721G>T, NM_001077446.3:c.721G>A, NM_001077446.3:c.721G>T, NM_001077446.2:c.721G>A, NM_001077446.2:c.721G>T, NM_001282332.2:c.721G>A, NM_001282332.2:c.721G>T, NM_001282332.1:c.721G>A, NM_001282332.1:c.721G>T, NM_001282333.2:c.721G>A, NM_001282333.2:c.721G>T, NM_001282333.1:c.730G>A, NM_001282333.1:c.730G>T, NM_001386740.1:c.721G>A, NM_001386740.1:c.721G>T, NG_015810.2:g.7115G>A, NG_015810.2:g.7115G>T, NW_003571061.2:g.167314G>A, NW_003571061.2:g.167314G>T, NW_003571059.2:g.167314G>A, NW_003571059.2:g.167314G>T, NW_003571058.2:g.167314G>A, NW_003571058.2:g.167314G>T, NW_003571057.2:g.167314G>A, NW_003571057.2:g.167314G>T, NW_003571056.2:g.167314G>A, NW_003571056.2:g.167314G>T, NW_003571055.2:g.167314G>A, NW_003571055.2:g.167314G>T, NW_003571061.1:g.167313G>A, NW_003571061.1:g.167313G>T, NW_003571060.1:g.167313G>A, NW_003571060.1:g.167313G>T, NW_003571054.1:g.167146G>A, NW_003571054.1:g.167146G>T, NT_187693.1:g.167314G>A, NT_187693.1:g.167314G>T, NC_000019.9:g.54696200G>A, NC_000019.9:g.54696200G>T, XM_011527294.4:c.721G>A, XM_011527294.4:c.721G>T, XM_011527294.3:c.721G>A, XM_011527294.3:c.721G>T, XM_011527294.2:c.721G>A, XM_011527294.2:c.721G>T, XM_011527294.1:c.721G>A, XM_011527294.1:c.721G>T, XM_047439391.1:c.721G>A, XM_047439391.1:c.721G>T, NP_076980.2:p.Gly241Arg, NP_076980.2:p.Gly241Ter, NP_001070914.1:p.Gly241Arg, NP_001070914.1:p.Gly241Ter, NP_001269261.1:p.Gly241Arg, NP_001269261.1:p.Gly241Ter, NP_001269262.2:p.Gly241Arg, NP_001269262.2:p.Gly241Ter, NP_001373669.1:p.Gly241Arg, NP_001373669.1:p.Gly241Ter, XP_011525596.1:p.Gly241Arg, XP_011525596.1:p.Gly241Ter, XP_047295347.1:p.Gly241Arg, XP_047295347.1:p.Gly241Ter

                              15.

                              rs1457973039 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                19:54193243 (GRCh38)
                                19:54697098 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:54193242:C:T
                                Gene:
                                TSEN34 (Varview)
                                Functional Consequence:
                                stop_gained,coding_sequence_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0./0 (ALFA)
                                T=0.000004/1 (TOPMED)
                                T=0.000007/1 (GnomAD)
                                HGVS:
                                NC_000019.10:g.54193243C>T, NW_004166865.1:g.167610C>T, NG_033045.2:g.1633G>A, NM_024075.5:c.814C>T, NM_024075.4:c.814C>T, NM_024075.3:c.814C>T, NM_001077446.4:c.814C>T, NM_001077446.3:c.814C>T, NM_001077446.2:c.814C>T, NM_001282332.2:c.814C>T, NM_001282332.1:c.814C>T, NM_001282333.2:c.814C>T, NM_001282333.1:c.823C>T, NM_001386740.1:c.814C>T, NG_015810.2:g.8009C>T, NW_003571061.2:g.168212C>T, NW_003571059.2:g.168212C>T, NW_003571058.2:g.168212C>T, NW_003571057.2:g.168212C>T, NW_003571056.2:g.168212C>T, NW_003571055.2:g.168212C>T, NW_003571061.1:g.168211C>T, NW_003571060.1:g.168206C>T, NW_003571054.1:g.168039C>T, NT_187693.1:g.168212C>T, NC_000019.9:g.54697098C>T, XM_011527294.4:c.814C>T, XM_011527294.3:c.814C>T, XM_011527294.2:c.814C>T, XM_011527294.1:c.814C>T, XM_047439391.1:c.814C>T, NP_076980.2:p.Gln272Ter, NP_001070914.1:p.Gln272Ter, NP_001269261.1:p.Gln272Ter, NP_001269262.2:p.Gln272Ter, NP_001373669.1:p.Gln272Ter, XP_011525596.1:p.Gln272Ter, XP_047295347.1:p.Gln272Ter

                                16.

                                rs1457690268 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>A,T [Show Flanks]
                                  Chromosome:
                                  19:54192119 (GRCh38)
                                  19:54695970 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:54192118:C:A,NC_000019.10:54192118:C:T
                                  Gene:
                                  TSEN34 (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,missense_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0./0 (ALFA)
                                  T=0.000004/1 (GnomAD_exomes)
                                  T=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000019.10:g.54192119C>A, NC_000019.10:g.54192119C>T, NW_004166865.1:g.166486C>A, NW_004166865.1:g.166486C>T, NG_033045.2:g.2757G>T, NG_033045.2:g.2757G>A, NM_024075.5:c.491C>A, NM_024075.5:c.491C>T, NM_024075.4:c.491C>A, NM_024075.4:c.491C>T, NM_024075.3:c.491C>A, NM_024075.3:c.491C>T, NM_001077446.4:c.491C>A, NM_001077446.4:c.491C>T, NM_001077446.3:c.491C>A, NM_001077446.3:c.491C>T, NM_001077446.2:c.491C>A, NM_001077446.2:c.491C>T, NM_001282332.2:c.491C>A, NM_001282332.2:c.491C>T, NM_001282332.1:c.491C>A, NM_001282332.1:c.491C>T, NM_001282333.2:c.491C>A, NM_001282333.2:c.491C>T, NM_001282333.1:c.500C>A, NM_001282333.1:c.500C>T, NM_001386740.1:c.491C>A, NM_001386740.1:c.491C>T, NG_015810.2:g.6885C>A, NG_015810.2:g.6885C>T, NW_003571061.2:g.167084C>A, NW_003571061.2:g.167084C>T, NW_003571059.2:g.167084C>A, NW_003571059.2:g.167084C>T, NW_003571058.2:g.167084C>A, NW_003571058.2:g.167084C>T, NW_003571057.2:g.167084C>A, NW_003571057.2:g.167084C>T, NW_003571056.2:g.167084C>A, NW_003571056.2:g.167084C>T, NW_003571055.2:g.167084C>A, NW_003571055.2:g.167084C>T, NW_003571061.1:g.167083C>A, NW_003571061.1:g.167083C>T, NW_003571060.1:g.167083C>A, NW_003571060.1:g.167083C>T, NW_003571054.1:g.166916C>A, NW_003571054.1:g.166916C>T, NT_187693.1:g.167084C>A, NT_187693.1:g.167084C>T, NC_000019.9:g.54695970C>A, NC_000019.9:g.54695970C>T, XM_011527294.4:c.491C>A, XM_011527294.4:c.491C>T, XM_011527294.3:c.491C>A, XM_011527294.3:c.491C>T, XM_011527294.2:c.491C>A, XM_011527294.2:c.491C>T, XM_011527294.1:c.491C>A, XM_011527294.1:c.491C>T, XM_047439391.1:c.491C>A, XM_047439391.1:c.491C>T, NP_076980.2:p.Pro164His, NP_076980.2:p.Pro164Leu, NP_001070914.1:p.Pro164His, NP_001070914.1:p.Pro164Leu, NP_001269261.1:p.Pro164His, NP_001269261.1:p.Pro164Leu, NP_001269262.2:p.Pro164His, NP_001269262.2:p.Pro164Leu, NP_001373669.1:p.Pro164His, NP_001373669.1:p.Pro164Leu, XP_011525596.1:p.Pro164His, XP_011525596.1:p.Pro164Leu, XP_047295347.1:p.Pro164His, XP_047295347.1:p.Pro164Leu

                                  17.

                                  rs1455142794 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    19:54191401 (GRCh38)
                                    19:54695252 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:54191400:G:T
                                    Gene:
                                    TSEN34 (Varview), MBOAT7 (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant,missense_variant
                                    HGVS:
                                    NC_000019.10:g.54191401G>T, NW_004166865.1:g.165768G>T, NG_033045.2:g.3475C>A, NM_024075.5:c.37G>T, NM_024075.4:c.37G>T, NM_024075.3:c.37G>T, NM_001077446.4:c.37G>T, NM_001077446.3:c.37G>T, NM_001077446.2:c.37G>T, NM_001282332.2:c.37G>T, NM_001282332.1:c.37G>T, NM_001282333.2:c.37G>T, NM_001282333.1:c.46G>T, NM_001386740.1:c.37G>T, NG_015810.2:g.6167G>T, NW_003571061.2:g.166366G>T, NW_003571059.2:g.166366G>T, NW_003571058.2:g.166366G>T, NW_003571057.2:g.166366G>T, NW_003571056.2:g.166366G>T, NW_003571055.2:g.166366G>T, NW_003571061.1:g.166365G>T, NW_003571060.1:g.166365G>T, NW_003571054.1:g.166198G>T, NT_187693.1:g.166366G>T, NC_000019.9:g.54695252G>T, XM_011527294.4:c.37G>T, XM_011527294.3:c.37G>T, XM_011527294.2:c.37G>T, XM_011527294.1:c.37G>T, XM_047439391.1:c.37G>T, NP_076980.2:p.Val13Leu, NP_001070914.1:p.Val13Leu, NP_001269261.1:p.Val13Leu, NP_001269262.2:p.Val13Leu, NP_001373669.1:p.Val13Leu, XP_011525596.1:p.Val13Leu, XP_047295347.1:p.Val13Leu

                                    18.

                                    rs1452664520 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      19:54193318 (GRCh38)
                                      19:54697173 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:54193317:G:A
                                      Gene:
                                      TSEN34 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      A=0./0 (ALFA)
                                      A=0.000007/1 (GnomAD)
                                      HGVS:
                                      NC_000019.10:g.54193318G>A, NW_004166865.1:g.167685G>A, NG_033045.2:g.1558C>T, NM_024075.5:c.889G>A, NM_024075.4:c.889G>A, NM_024075.3:c.889G>A, NM_001077446.4:c.889G>A, NM_001077446.3:c.889G>A, NM_001077446.2:c.889G>A, NM_001282332.2:c.889G>A, NM_001282332.1:c.889G>A, NM_001282333.2:c.889G>A, NM_001282333.1:c.898G>A, NM_001386740.1:c.889G>A, NG_015810.2:g.8084G>A, NW_003571061.2:g.168287G>A, NW_003571059.2:g.168287G>A, NW_003571058.2:g.168287G>A, NW_003571057.2:g.168287G>A, NW_003571056.2:g.168287G>A, NW_003571055.2:g.168287G>A, NW_003571061.1:g.168286G>A, NW_003571060.1:g.168281G>A, NW_003571054.1:g.168114G>A, NT_187693.1:g.168287G>A, NC_000019.9:g.54697173G>A, XM_011527294.4:c.889G>A, XM_011527294.3:c.889G>A, XM_011527294.2:c.889G>A, XM_011527294.1:c.889G>A, XM_047439391.1:c.889G>A, NP_076980.2:p.Gly297Ser, NP_001070914.1:p.Gly297Ser, NP_001269261.1:p.Gly297Ser, NP_001269262.2:p.Gly297Arg, NP_001373669.1:p.Gly297Ser, XP_011525596.1:p.Gly297Ser, XP_047295347.1:p.Gly297Ser

                                      19.

                                      rs1452498569 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>C [Show Flanks]
                                        Chromosome:
                                        19:54191852 (GRCh38)
                                        19:54695703 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:54191851:G:C
                                        Gene:
                                        TSEN34 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,missense_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        C=0./0 (ALFA)
                                        C=0.000004/1 (TOPMED)
                                        HGVS:
                                        NC_000019.10:g.54191852G>C, NW_004166865.1:g.166219G>C, NG_033045.2:g.3024C>G, NM_024075.5:c.375G>C, NM_024075.4:c.375G>C, NM_024075.3:c.375G>C, NM_001077446.4:c.375G>C, NM_001077446.3:c.375G>C, NM_001077446.2:c.375G>C, NM_001282332.2:c.375G>C, NM_001282332.1:c.375G>C, NM_001282333.2:c.375G>C, NM_001282333.1:c.384G>C, NM_001386740.1:c.375G>C, NG_015810.2:g.6618G>C, NW_003571061.2:g.166817G>C, NW_003571059.2:g.166817G>C, NW_003571058.2:g.166817G>C, NW_003571057.2:g.166817G>C, NW_003571056.2:g.166817G>C, NW_003571055.2:g.166817G>C, NW_003571061.1:g.166816G>C, NW_003571060.1:g.166816G>C, NW_003571054.1:g.166649G>C, NT_187693.1:g.166817G>C, NC_000019.9:g.54695703G>C, XM_011527294.4:c.375G>C, XM_011527294.3:c.375G>C, XM_011527294.2:c.375G>C, XM_011527294.1:c.375G>C, XM_047439391.1:c.375G>C, NP_076980.2:p.Gln125His, NP_001070914.1:p.Gln125His, NP_001269261.1:p.Gln125His, NP_001269262.2:p.Gln125His, NP_001373669.1:p.Gln125His, XP_011525596.1:p.Gln125His, XP_047295347.1:p.Gln125His

                                        20.

                                        rs1451603451 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          19:54193345 (GRCh38)
                                          19:54697200 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:54193344:T:C
                                          Gene:
                                          TSEN34 (Varview)
                                          Functional Consequence:
                                          intron_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_000019.10:g.54193345T>C, NW_004166865.1:g.167712T>C, NG_033045.2:g.1531A>G, NM_024075.5:c.916T>C, NM_024075.4:c.916T>C, NM_024075.3:c.916T>C, NM_001077446.4:c.916T>C, NM_001077446.3:c.916T>C, NM_001077446.2:c.916T>C, NM_001282332.2:c.916T>C, NM_001282332.1:c.916T>C, NM_001386740.1:c.916T>C, NG_015810.2:g.8111T>C, NW_003571061.2:g.168314T>C, NW_003571059.2:g.168314T>C, NW_003571058.2:g.168314T>C, NW_003571057.2:g.168314T>C, NW_003571056.2:g.168314T>C, NW_003571055.2:g.168314T>C, NW_003571061.1:g.168313T>C, NW_003571060.1:g.168308T>C, NW_003571054.1:g.168141T>C, NT_187693.1:g.168314T>C, NC_000019.9:g.54697200T>C, XM_011527294.4:c.916T>C, XM_011527294.3:c.916T>C, XM_011527294.2:c.916T>C, XM_011527294.1:c.916T>C, XM_047439391.1:c.916T>C, NP_076980.2:p.Trp306Arg, NP_001070914.1:p.Trp306Arg, NP_001269261.1:p.Trp306Arg, NP_001373669.1:p.Trp306Arg, XP_011525596.1:p.Trp306Arg, XP_047295347.1:p.Trp306Arg

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...