Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Protein

Items: 1 to 20 of 834

9.
12.

rs781033550 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>A,G [Show Flanks]
    Chromosome:
    17:8490349 (GRCh38)
    17:8393667 (GRCh37)
    Canonical SPDI:
    NC_000017.11:8490348:C:A,NC_000017.11:8490348:C:G
    Gene:
    MYH10 (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0./0 (ALFA)
    A=0.000004/1 (GnomAD_exomes)
    G=0.000004/1 (TOPMED)
    A=0.000008/1 (ExAC)
    HGVS:
    NC_000017.11:g.8490349C>A, NC_000017.11:g.8490349C>G, NC_000017.10:g.8393667C>A, NC_000017.10:g.8393667C>G, NG_042305.2:g.145413G>T, NG_042305.2:g.145413G>C, NG_042305.1:g.145413G>T, NG_042305.1:g.145413G>C, NM_005964.5:c.4782G>T, NM_005964.5:c.4782G>C, NM_005964.4:c.4782G>T, NM_005964.4:c.4782G>C, NM_005964.3:c.4782G>T, NM_005964.3:c.4782G>C, NM_001256012.3:c.4875G>T, NM_001256012.3:c.4875G>C, NM_001256012.2:c.4875G>T, NM_001256012.2:c.4875G>C, NM_001256012.1:c.4875G>T, NM_001256012.1:c.4875G>C, NM_001256095.2:c.4809G>T, NM_001256095.2:c.4809G>C, NM_001256095.1:c.4809G>T, NM_001256095.1:c.4809G>C, NM_001375266.1:c.4812G>T, NM_001375266.1:c.4812G>C, XM_011523875.2:c.4965G>T, XM_011523875.2:c.4965G>C, XM_011523878.2:c.4902G>T, XM_011523878.2:c.4902G>C, XM_011523879.2:c.4899G>T, XM_011523879.2:c.4899G>C, XM_011523880.2:c.4872G>T, XM_011523880.2:c.4872G>C, XM_017024680.1:c.4809G>T, XM_017024680.1:c.4809G>C, XM_017024679.1:c.4812G>T, XM_017024679.1:c.4812G>C, XM_017024678.1:c.4812G>T, XM_017024678.1:c.4812G>C, XM_017024681.1:c.4782G>T, XM_017024681.1:c.4782G>C, XM_017024682.1:c.4782G>T, XM_017024682.1:c.4782G>C
    14.

    rs781018741 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>T [Show Flanks]
      Chromosome:
      17:8535929 (GRCh38)
      17:8439247 (GRCh37)
      Canonical SPDI:
      NC_000017.11:8535928:C:T
      Gene:
      MYH10 (Varview)
      Functional Consequence:
      synonymous_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      T=0./0 (ALFA)
      T=0.000008/1 (ExAC)
      T=0.000011/3 (TOPMED)
      T=0.000012/3 (GnomAD_exomes)
      T=0.000014/2 (GnomAD)
      HGVS:
      18.

      rs780658326 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        17:8499357 (GRCh38)
        17:8402675 (GRCh37)
        Canonical SPDI:
        NC_000017.11:8499356:G:A
        Gene:
        MYH10 (Varview)
        Functional Consequence:
        synonymous_variant,coding_sequence_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0.000071/1 (ALFA)
        A=0.000008/1 (ExAC)
        A=0.000008/2 (GnomAD_exomes)
        A=0.000021/3 (GnomAD)
        A=0.00003/8 (TOPMED)
        HGVS:
        19.

        rs780650576 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A,C [Show Flanks]
          Chromosome:
          17:8478367 (GRCh38)
          17:8381685 (GRCh37)
          Canonical SPDI:
          NC_000017.11:8478366:G:A,NC_000017.11:8478366:G:C
          Gene:
          MYH10 (Varview)
          Functional Consequence:
          missense_variant,coding_sequence_variant
          Validated:
          by frequency,by cluster
          MAF:
          A=0.000007/1 (GnomAD)
          HGVS:
          NC_000017.11:g.8478367G>A, NC_000017.11:g.8478367G>C, NC_000017.10:g.8381685G>A, NC_000017.10:g.8381685G>C, NG_042305.2:g.157395C>T, NG_042305.2:g.157395C>G, NG_042305.1:g.157395C>T, NG_042305.1:g.157395C>G, NM_005964.5:c.5584C>T, NM_005964.5:c.5584C>G, NM_005964.4:c.5584C>T, NM_005964.4:c.5584C>G, NM_005964.3:c.5584C>T, NM_005964.3:c.5584C>G, NM_001256012.3:c.5677C>T, NM_001256012.3:c.5677C>G, NM_001256012.2:c.5677C>T, NM_001256012.2:c.5677C>G, NM_001256012.1:c.5677C>T, NM_001256012.1:c.5677C>G, NM_001256095.2:c.5611C>T, NM_001256095.2:c.5611C>G, NM_001256095.1:c.5611C>T, NM_001256095.1:c.5611C>G, NM_001375266.1:c.5614C>T, NM_001375266.1:c.5614C>G, XM_011523875.2:c.5767C>T, XM_011523875.2:c.5767C>G, XM_011523878.2:c.5704C>T, XM_011523878.2:c.5704C>G, XM_011523879.2:c.5701C>T, XM_011523879.2:c.5701C>G, XM_011523880.2:c.5674C>T, XM_011523880.2:c.5674C>G, XM_017024680.1:c.5611C>T, XM_017024680.1:c.5611C>G, XM_017024679.1:c.5614C>T, XM_017024679.1:c.5614C>G, XM_017024678.1:c.5614C>T, XM_017024678.1:c.5614C>G, XM_017024681.1:c.5584C>T, XM_017024681.1:c.5584C>G, XM_017024682.1:c.5584C>T, XM_017024682.1:c.5584C>G, NP_005955.3:p.Arg1862Cys, NP_005955.3:p.Arg1862Gly, NP_001242941.1:p.Arg1893Cys, NP_001242941.1:p.Arg1893Gly, NP_001243024.1:p.Arg1871Cys, NP_001243024.1:p.Arg1871Gly, NP_001362195.1:p.Arg1872Cys, NP_001362195.1:p.Arg1872Gly, XP_011522177.1:p.Arg1923Cys, XP_011522177.1:p.Arg1923Gly, XP_011522180.1:p.Arg1902Cys, XP_011522180.1:p.Arg1902Gly, XP_011522181.1:p.Arg1901Cys, XP_011522181.1:p.Arg1901Gly, XP_011522182.1:p.Arg1892Cys, XP_011522182.1:p.Arg1892Gly, XP_016880169.1:p.Arg1871Cys, XP_016880169.1:p.Arg1871Gly, XP_016880168.1:p.Arg1872Cys, XP_016880168.1:p.Arg1872Gly, XP_016880167.1:p.Arg1872Cys, XP_016880167.1:p.Arg1872Gly, XP_016880170.1:p.Arg1862Cys, XP_016880170.1:p.Arg1862Gly, XP_016880171.1:p.Arg1862Cys, XP_016880171.1:p.Arg1862Gly

          Display Settings:

          Format
          Items per page
          Sort by

          Send to:

          Choose Destination

          Supplemental Content

          Find related data

          Recent activity

          Your browsing activity is empty.

          Activity recording is turned off.

          Turn recording back on

          See more...
          Support Center