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Items: 1 to 20 of 264

1.

rs1490838516 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    11:1934604 (GRCh38)
    11:1955834 (GRCh37)
    Canonical SPDI:
    NC_000011.10:1934603:C:T
    Gene:
    TNNT3 (Varview)
    Functional Consequence:
    missense_variant,coding_sequence_variant
    HGVS:
    NC_000011.10:g.1934604C>T, NC_000011.9:g.1955834C>T, NW_021160004.1:g.103432C>T, XM_006718294.4:c.548C>T, XM_006718294.3:c.548C>T, XM_006718294.2:c.548C>T, XM_006718294.1:c.548C>T, NM_006757.4:c.539C>T, NM_006757.3:c.539C>T, XM_006718300.4:c.500C>T, XM_006718300.3:c.500C>T, XM_006718300.2:c.500C>T, XM_006718300.1:c.500C>T, XM_011520343.3:c.572C>T, XM_011520343.2:c.572C>T, XM_011520343.1:c.572C>T, NM_001042781.3:c.533C>T, NM_001042781.2:c.533C>T, NM_001042782.3:c.515C>T, NM_001042782.2:c.515C>T, NM_001042780.3:c.515C>T, NM_001042780.2:c.515C>T, XM_006718299.3:c.512C>T, XM_006718299.2:c.512C>T, XM_006718299.1:c.512C>T, NM_001297646.2:c.515C>T, NM_001297646.1:c.515C>T, XM_017018216.2:c.554C>T, XM_017018216.1:c.554C>T, NM_001363561.2:c.548C>T, NM_001363561.1:c.548C>T, XM_017018206.2:c.572C>T, XM_017018206.1:c.572C>T, XM_017018217.2:c.533C>T, XM_017018217.1:c.533C>T, XM_017018205.2:c.533C>T, XM_017018205.1:c.533C>T, XM_017018207.2:c.560C>T, XM_017018207.1:c.560C>T, XM_017018218.2:c.521C>T, XM_017018218.1:c.521C>T, XM_017018209.2:c.536C>T, XM_017018209.1:c.536C>T, XM_024448669.2:c.533C>T, XM_024448669.1:c.533C>T, XM_017018208.2:c.551C>T, XM_017018208.1:c.551C>T, XM_017018219.2:c.482C>T, XM_017018219.1:c.482C>T, XM_017018211.2:c.521C>T, XM_017018211.1:c.521C>T, XM_017018210.2:c.527C>T, XM_017018210.1:c.527C>T, XM_017018212.2:c.518C>T, XM_017018212.1:c.518C>T, XM_024448670.2:c.515C>T, XM_024448670.1:c.515C>T, XM_024448671.2:c.512C>T, XM_024448671.1:c.512C>T, XM_017018213.2:c.503C>T, XM_017018213.1:c.503C>T, XM_017018214.2:c.500C>T, XM_017018214.1:c.500C>T, XM_024448672.2:c.494C>T, XM_024448672.1:c.494C>T, XM_017018215.2:c.494C>T, XM_017018215.1:c.494C>T, NM_001367846.1:c.572C>T, NM_001367848.1:c.536C>T, NM_001367843.1:c.533C>T, NM_001367845.1:c.515C>T, NM_001367847.1:c.548C>T, NM_001367842.1:c.533C>T, NM_001367850.1:c.482C>T, NM_001367844.1:c.515C>T, NM_001367851.1:c.335C>T, NM_001367852.1:c.335C>T, NM_001367849.1:c.527C>T, XP_006718357.1:p.Ala183Val, NP_006748.1:p.Ala180Val, XP_006718363.1:p.Ala167Val, XP_011518645.1:p.Ala191Val, NP_001036246.1:p.Ala178Val, NP_001036247.1:p.Ala172Val, NP_001036245.1:p.Ala172Val, XP_006718362.1:p.Ala171Val, NP_001284575.1:p.Ala172Val, XP_016873705.1:p.Ala185Val, NP_001350490.1:p.Ala183Val, XP_016873695.1:p.Ala191Val, XP_016873706.1:p.Ala178Val, XP_016873694.1:p.Ala178Val, XP_016873696.1:p.Ala187Val, XP_016873707.1:p.Ala174Val, XP_016873698.1:p.Ala179Val, XP_024304437.1:p.Ala178Val, XP_016873697.1:p.Ala184Val, XP_016873708.1:p.Ala161Val, XP_016873700.1:p.Ala174Val, XP_016873699.1:p.Ala176Val, XP_016873701.1:p.Ala173Val, XP_024304438.1:p.Ala172Val, XP_024304439.1:p.Ala171Val, XP_016873702.1:p.Ala168Val, XP_016873703.1:p.Ala167Val, XP_024304440.1:p.Ala165Val, XP_016873704.1:p.Ala165Val, NP_001354775.1:p.Ala191Val, NP_001354777.1:p.Ala179Val, NP_001354772.1:p.Ala178Val, NP_001354774.1:p.Ala172Val, NP_001354776.1:p.Ala183Val, NP_001354771.1:p.Ala178Val, NP_001354779.1:p.Ala161Val, NP_001354773.1:p.Ala172Val, NP_001354780.1:p.Ala112Val, NP_001354781.1:p.Ala112Val, NP_001354778.1:p.Ala176Val

    2.

    rs1485624802 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>A,T [Show Flanks]
      Chromosome:
      11:1934003 (GRCh38)
      11:1955233 (GRCh37)
      Canonical SPDI:
      NC_000011.10:1934002:C:A,NC_000011.10:1934002:C:T
      Gene:
      TNNT3 (Varview)
      Functional Consequence:
      missense_variant,coding_sequence_variant,synonymous_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0.000066/1 (ALFA)
      T=0.000004/1 (TOPMED)
      A=0.000007/1 (GnomAD)
      A=0.000223/1 (Estonian)
      HGVS:
      NC_000011.10:g.1934003C>A, NC_000011.10:g.1934003C>T, NC_000011.9:g.1955233C>A, NC_000011.9:g.1955233C>T, NW_021160004.1:g.102831C>A, NW_021160004.1:g.102831C>T, XM_006718294.4:c.370C>A, XM_006718294.4:c.370C>T, XM_006718294.3:c.370C>A, XM_006718294.3:c.370C>T, XM_006718294.2:c.370C>A, XM_006718294.2:c.370C>T, XM_006718294.1:c.370C>A, XM_006718294.1:c.370C>T, NM_006757.4:c.361C>A, NM_006757.4:c.361C>T, NM_006757.3:c.361C>A, NM_006757.3:c.361C>T, XM_006718300.4:c.322C>A, XM_006718300.4:c.322C>T, XM_006718300.3:c.322C>A, XM_006718300.3:c.322C>T, XM_006718300.2:c.322C>A, XM_006718300.2:c.322C>T, XM_006718300.1:c.322C>A, XM_006718300.1:c.322C>T, XM_011520343.3:c.394C>A, XM_011520343.3:c.394C>T, XM_011520343.2:c.394C>A, XM_011520343.2:c.394C>T, XM_011520343.1:c.394C>A, XM_011520343.1:c.394C>T, NM_001042781.3:c.355C>A, NM_001042781.3:c.355C>T, NM_001042781.2:c.355C>A, NM_001042781.2:c.355C>T, NM_001042782.3:c.337C>A, NM_001042782.3:c.337C>T, NM_001042782.2:c.337C>A, NM_001042782.2:c.337C>T, NM_001042780.3:c.337C>A, NM_001042780.3:c.337C>T, NM_001042780.2:c.337C>A, NM_001042780.2:c.337C>T, XM_006718299.3:c.334C>A, XM_006718299.3:c.334C>T, XM_006718299.2:c.334C>A, XM_006718299.2:c.334C>T, XM_006718299.1:c.334C>A, XM_006718299.1:c.334C>T, NM_001297646.2:c.337C>A, NM_001297646.2:c.337C>T, NM_001297646.1:c.337C>A, NM_001297646.1:c.337C>T, XM_017018216.2:c.376C>A, XM_017018216.2:c.376C>T, XM_017018216.1:c.376C>A, XM_017018216.1:c.376C>T, NM_001363561.2:c.370C>A, NM_001363561.2:c.370C>T, NM_001363561.1:c.370C>A, NM_001363561.1:c.370C>T, XM_017018206.2:c.394C>A, XM_017018206.2:c.394C>T, XM_017018206.1:c.394C>A, XM_017018206.1:c.394C>T, XM_017018217.2:c.355C>A, XM_017018217.2:c.355C>T, XM_017018217.1:c.355C>A, XM_017018217.1:c.355C>T, XM_017018205.2:c.355C>A, XM_017018205.2:c.355C>T, XM_017018205.1:c.355C>A, XM_017018205.1:c.355C>T, XM_017018207.2:c.382C>A, XM_017018207.2:c.382C>T, XM_017018207.1:c.382C>A, XM_017018207.1:c.382C>T, XM_017018218.2:c.343C>A, XM_017018218.2:c.343C>T, XM_017018218.1:c.343C>A, XM_017018218.1:c.343C>T, XM_017018209.2:c.358C>A, XM_017018209.2:c.358C>T, XM_017018209.1:c.358C>A, XM_017018209.1:c.358C>T, XM_024448669.2:c.355C>A, XM_024448669.2:c.355C>T, XM_024448669.1:c.355C>A, XM_024448669.1:c.355C>T, XM_017018208.2:c.373C>A, XM_017018208.2:c.373C>T, XM_017018208.1:c.373C>A, XM_017018208.1:c.373C>T, XM_017018219.2:c.304C>A, XM_017018219.2:c.304C>T, XM_017018219.1:c.304C>A, XM_017018219.1:c.304C>T, XM_017018211.2:c.343C>A, XM_017018211.2:c.343C>T, XM_017018211.1:c.343C>A, XM_017018211.1:c.343C>T, XM_017018210.2:c.349C>A, XM_017018210.2:c.349C>T, XM_017018210.1:c.349C>A, XM_017018210.1:c.349C>T, XM_017018212.2:c.340C>A, XM_017018212.2:c.340C>T, XM_017018212.1:c.340C>A, XM_017018212.1:c.340C>T, XM_024448670.2:c.337C>A, XM_024448670.2:c.337C>T, XM_024448670.1:c.337C>A, XM_024448670.1:c.337C>T, XM_024448671.2:c.334C>A, XM_024448671.2:c.334C>T, XM_024448671.1:c.334C>A, XM_024448671.1:c.334C>T, XM_017018213.2:c.325C>A, XM_017018213.2:c.325C>T, XM_017018213.1:c.325C>A, XM_017018213.1:c.325C>T, XM_017018214.2:c.322C>A, XM_017018214.2:c.322C>T, XM_017018214.1:c.322C>A, XM_017018214.1:c.322C>T, XM_024448672.2:c.316C>A, XM_024448672.2:c.316C>T, XM_024448672.1:c.316C>A, XM_024448672.1:c.316C>T, XM_017018215.2:c.316C>A, XM_017018215.2:c.316C>T, XM_017018215.1:c.316C>A, XM_017018215.1:c.316C>T, NM_001367846.1:c.394C>A, NM_001367846.1:c.394C>T, NM_001367848.1:c.358C>A, NM_001367848.1:c.358C>T, NM_001367843.1:c.355C>A, NM_001367843.1:c.355C>T, NM_001367845.1:c.337C>A, NM_001367845.1:c.337C>T, NM_001367847.1:c.370C>A, NM_001367847.1:c.370C>T, NM_001367842.1:c.355C>A, NM_001367842.1:c.355C>T, NM_001367850.1:c.304C>A, NM_001367850.1:c.304C>T, NM_001367844.1:c.337C>A, NM_001367844.1:c.337C>T, NM_001367851.1:c.157C>A, NM_001367851.1:c.157C>T, NM_001367852.1:c.157C>A, NM_001367852.1:c.157C>T, NM_001367849.1:c.349C>A, NM_001367849.1:c.349C>T, XP_006718357.1:p.Leu124Met, NP_006748.1:p.Leu121Met, XP_006718363.1:p.Leu108Met, XP_011518645.1:p.Leu132Met, NP_001036246.1:p.Leu119Met, NP_001036247.1:p.Leu113Met, NP_001036245.1:p.Leu113Met, XP_006718362.1:p.Leu112Met, NP_001284575.1:p.Leu113Met, XP_016873705.1:p.Leu126Met, NP_001350490.1:p.Leu124Met, XP_016873695.1:p.Leu132Met, XP_016873706.1:p.Leu119Met, XP_016873694.1:p.Leu119Met, XP_016873696.1:p.Leu128Met, XP_016873707.1:p.Leu115Met, XP_016873698.1:p.Leu120Met, XP_024304437.1:p.Leu119Met, XP_016873697.1:p.Leu125Met, XP_016873708.1:p.Leu102Met, XP_016873700.1:p.Leu115Met, XP_016873699.1:p.Leu117Met, XP_016873701.1:p.Leu114Met, XP_024304438.1:p.Leu113Met, XP_024304439.1:p.Leu112Met, XP_016873702.1:p.Leu109Met, XP_016873703.1:p.Leu108Met, XP_024304440.1:p.Leu106Met, XP_016873704.1:p.Leu106Met, NP_001354775.1:p.Leu132Met, NP_001354777.1:p.Leu120Met, NP_001354772.1:p.Leu119Met, NP_001354774.1:p.Leu113Met, NP_001354776.1:p.Leu124Met, NP_001354771.1:p.Leu119Met, NP_001354779.1:p.Leu102Met, NP_001354773.1:p.Leu113Met, NP_001354780.1:p.Leu53Met, NP_001354781.1:p.Leu53Met, NP_001354778.1:p.Leu117Met

      3.

      rs1483995222 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        11:1934591 (GRCh38)
        11:1955821 (GRCh37)
        Canonical SPDI:
        NC_000011.10:1934590:A:G
        Gene:
        TNNT3 (Varview)
        Functional Consequence:
        coding_sequence_variant,missense_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0./0 (ALFA)
        G=0.000004/1 (TOPMED)
        G=0.000007/1 (GnomAD)
        HGVS:
        NC_000011.10:g.1934591A>G, NC_000011.9:g.1955821A>G, NW_021160004.1:g.103419A>G, XM_006718294.4:c.535A>G, XM_006718294.3:c.535A>G, XM_006718294.2:c.535A>G, XM_006718294.1:c.535A>G, NM_006757.4:c.526A>G, NM_006757.3:c.526A>G, XM_006718300.4:c.487A>G, XM_006718300.3:c.487A>G, XM_006718300.2:c.487A>G, XM_006718300.1:c.487A>G, XM_011520343.3:c.559A>G, XM_011520343.2:c.559A>G, XM_011520343.1:c.559A>G, NM_001042781.3:c.520A>G, NM_001042781.2:c.520A>G, NM_001042782.3:c.502A>G, NM_001042782.2:c.502A>G, NM_001042780.3:c.502A>G, NM_001042780.2:c.502A>G, XM_006718299.3:c.499A>G, XM_006718299.2:c.499A>G, XM_006718299.1:c.499A>G, NM_001297646.2:c.502A>G, NM_001297646.1:c.502A>G, XM_017018216.2:c.541A>G, XM_017018216.1:c.541A>G, NM_001363561.2:c.535A>G, NM_001363561.1:c.535A>G, XM_017018206.2:c.559A>G, XM_017018206.1:c.559A>G, XM_017018217.2:c.520A>G, XM_017018217.1:c.520A>G, XM_017018205.2:c.520A>G, XM_017018205.1:c.520A>G, XM_017018207.2:c.547A>G, XM_017018207.1:c.547A>G, XM_017018218.2:c.508A>G, XM_017018218.1:c.508A>G, XM_017018209.2:c.523A>G, XM_017018209.1:c.523A>G, XM_024448669.2:c.520A>G, XM_024448669.1:c.520A>G, XM_017018208.2:c.538A>G, XM_017018208.1:c.538A>G, XM_017018219.2:c.469A>G, XM_017018219.1:c.469A>G, XM_017018211.2:c.508A>G, XM_017018211.1:c.508A>G, XM_017018210.2:c.514A>G, XM_017018210.1:c.514A>G, XM_017018212.2:c.505A>G, XM_017018212.1:c.505A>G, XM_024448670.2:c.502A>G, XM_024448670.1:c.502A>G, XM_024448671.2:c.499A>G, XM_024448671.1:c.499A>G, XM_017018213.2:c.490A>G, XM_017018213.1:c.490A>G, XM_017018214.2:c.487A>G, XM_017018214.1:c.487A>G, XM_024448672.2:c.481A>G, XM_024448672.1:c.481A>G, XM_017018215.2:c.481A>G, XM_017018215.1:c.481A>G, NM_001367846.1:c.559A>G, NM_001367848.1:c.523A>G, NM_001367843.1:c.520A>G, NM_001367845.1:c.502A>G, NM_001367847.1:c.535A>G, NM_001367842.1:c.520A>G, NM_001367850.1:c.469A>G, NM_001367844.1:c.502A>G, NM_001367851.1:c.322A>G, NM_001367852.1:c.322A>G, NM_001367849.1:c.514A>G, XP_006718357.1:p.Lys179Glu, NP_006748.1:p.Lys176Glu, XP_006718363.1:p.Lys163Glu, XP_011518645.1:p.Lys187Glu, NP_001036246.1:p.Lys174Glu, NP_001036247.1:p.Lys168Glu, NP_001036245.1:p.Lys168Glu, XP_006718362.1:p.Lys167Glu, NP_001284575.1:p.Lys168Glu, XP_016873705.1:p.Lys181Glu, NP_001350490.1:p.Lys179Glu, XP_016873695.1:p.Lys187Glu, XP_016873706.1:p.Lys174Glu, XP_016873694.1:p.Lys174Glu, XP_016873696.1:p.Lys183Glu, XP_016873707.1:p.Lys170Glu, XP_016873698.1:p.Lys175Glu, XP_024304437.1:p.Lys174Glu, XP_016873697.1:p.Lys180Glu, XP_016873708.1:p.Lys157Glu, XP_016873700.1:p.Lys170Glu, XP_016873699.1:p.Lys172Glu, XP_016873701.1:p.Lys169Glu, XP_024304438.1:p.Lys168Glu, XP_024304439.1:p.Lys167Glu, XP_016873702.1:p.Lys164Glu, XP_016873703.1:p.Lys163Glu, XP_024304440.1:p.Lys161Glu, XP_016873704.1:p.Lys161Glu, NP_001354775.1:p.Lys187Glu, NP_001354777.1:p.Lys175Glu, NP_001354772.1:p.Lys174Glu, NP_001354774.1:p.Lys168Glu, NP_001354776.1:p.Lys179Glu, NP_001354771.1:p.Lys174Glu, NP_001354779.1:p.Lys157Glu, NP_001354773.1:p.Lys168Glu, NP_001354780.1:p.Lys108Glu, NP_001354781.1:p.Lys108Glu, NP_001354778.1:p.Lys172Glu

        4.

        rs1483488484 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>A [Show Flanks]
          Chromosome:
          11:1934614 (GRCh38)
          11:1955844 (GRCh37)
          Canonical SPDI:
          NC_000011.10:1934613:C:A
          Gene:
          TNNT3 (Varview)
          Functional Consequence:
          coding_sequence_variant,synonymous_variant
          HGVS:
          NC_000011.10:g.1934614C>A, NC_000011.9:g.1955844C>A, NW_021160004.1:g.103442C>A, XM_006718294.4:c.558C>A, XM_006718294.3:c.558C>A, XM_006718294.2:c.558C>A, XM_006718294.1:c.558C>A, NM_006757.4:c.549C>A, NM_006757.3:c.549C>A, XM_006718300.4:c.510C>A, XM_006718300.3:c.510C>A, XM_006718300.2:c.510C>A, XM_006718300.1:c.510C>A, XM_011520343.3:c.582C>A, XM_011520343.2:c.582C>A, XM_011520343.1:c.582C>A, NM_001042781.3:c.543C>A, NM_001042781.2:c.543C>A, NM_001042782.3:c.525C>A, NM_001042782.2:c.525C>A, NM_001042780.3:c.525C>A, NM_001042780.2:c.525C>A, XM_006718299.3:c.522C>A, XM_006718299.2:c.522C>A, XM_006718299.1:c.522C>A, NM_001297646.2:c.525C>A, NM_001297646.1:c.525C>A, XM_017018216.2:c.564C>A, XM_017018216.1:c.564C>A, NM_001363561.2:c.558C>A, NM_001363561.1:c.558C>A, XM_017018206.2:c.582C>A, XM_017018206.1:c.582C>A, XM_017018217.2:c.543C>A, XM_017018217.1:c.543C>A, XM_017018205.2:c.543C>A, XM_017018205.1:c.543C>A, XM_017018207.2:c.570C>A, XM_017018207.1:c.570C>A, XM_017018218.2:c.531C>A, XM_017018218.1:c.531C>A, XM_017018209.2:c.546C>A, XM_017018209.1:c.546C>A, XM_024448669.2:c.543C>A, XM_024448669.1:c.543C>A, XM_017018208.2:c.561C>A, XM_017018208.1:c.561C>A, XM_017018219.2:c.492C>A, XM_017018219.1:c.492C>A, XM_017018211.2:c.531C>A, XM_017018211.1:c.531C>A, XM_017018210.2:c.537C>A, XM_017018210.1:c.537C>A, XM_017018212.2:c.528C>A, XM_017018212.1:c.528C>A, XM_024448670.2:c.525C>A, XM_024448670.1:c.525C>A, XM_024448671.2:c.522C>A, XM_024448671.1:c.522C>A, XM_017018213.2:c.513C>A, XM_017018213.1:c.513C>A, XM_017018214.2:c.510C>A, XM_017018214.1:c.510C>A, XM_024448672.2:c.504C>A, XM_024448672.1:c.504C>A, XM_017018215.2:c.504C>A, XM_017018215.1:c.504C>A, NM_001367846.1:c.582C>A, NM_001367848.1:c.546C>A, NM_001367843.1:c.543C>A, NM_001367845.1:c.525C>A, NM_001367847.1:c.558C>A, NM_001367842.1:c.543C>A, NM_001367850.1:c.492C>A, NM_001367844.1:c.525C>A, NM_001367851.1:c.345C>A, NM_001367852.1:c.345C>A, NM_001367849.1:c.537C>A

          5.

          rs1483036041 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>A [Show Flanks]
            Chromosome:
            11:1933791 (GRCh38)
            11:1955021 (GRCh37)
            Canonical SPDI:
            NC_000011.10:1933790:C:A
            Gene:
            TNNT3 (Varview)
            Functional Consequence:
            coding_sequence_variant,missense_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            A=0./0 (ALFA)
            A=0.000004/1 (GnomAD_exomes)
            A=0.000004/1 (TOPMED)
            HGVS:
            NC_000011.10:g.1933791C>A, NC_000011.9:g.1955021C>A, NW_021160004.1:g.102619C>A, XM_006718294.4:c.251C>A, XM_006718294.3:c.251C>A, XM_006718294.2:c.251C>A, XM_006718294.1:c.251C>A, NM_006757.4:c.242C>A, NM_006757.3:c.242C>A, XM_006718300.4:c.203C>A, XM_006718300.3:c.203C>A, XM_006718300.2:c.203C>A, XM_006718300.1:c.203C>A, XM_011520343.3:c.275C>A, XM_011520343.2:c.275C>A, XM_011520343.1:c.275C>A, NM_001042781.3:c.236C>A, NM_001042781.2:c.236C>A, NM_001042782.3:c.218C>A, NM_001042782.2:c.218C>A, NM_001042780.3:c.218C>A, NM_001042780.2:c.218C>A, XM_006718299.3:c.215C>A, XM_006718299.2:c.215C>A, XM_006718299.1:c.215C>A, NM_001297646.2:c.218C>A, NM_001297646.1:c.218C>A, XM_017018216.2:c.257C>A, XM_017018216.1:c.257C>A, NM_001363561.2:c.251C>A, NM_001363561.1:c.251C>A, XM_017018206.2:c.275C>A, XM_017018206.1:c.275C>A, XM_017018217.2:c.236C>A, XM_017018217.1:c.236C>A, XM_017018205.2:c.236C>A, XM_017018205.1:c.236C>A, XM_017018207.2:c.263C>A, XM_017018207.1:c.263C>A, XM_017018218.2:c.224C>A, XM_017018218.1:c.224C>A, XM_017018209.2:c.239C>A, XM_017018209.1:c.239C>A, XM_024448669.2:c.236C>A, XM_024448669.1:c.236C>A, XM_017018208.2:c.254C>A, XM_017018208.1:c.254C>A, XM_017018219.2:c.185C>A, XM_017018219.1:c.185C>A, XM_017018211.2:c.224C>A, XM_017018211.1:c.224C>A, XM_017018210.2:c.230C>A, XM_017018210.1:c.230C>A, XM_017018212.2:c.221C>A, XM_017018212.1:c.221C>A, XM_024448670.2:c.218C>A, XM_024448670.1:c.218C>A, XM_024448671.2:c.215C>A, XM_024448671.1:c.215C>A, XM_017018213.2:c.206C>A, XM_017018213.1:c.206C>A, XM_017018214.2:c.203C>A, XM_017018214.1:c.203C>A, XM_024448672.2:c.197C>A, XM_024448672.1:c.197C>A, XM_017018215.2:c.197C>A, XM_017018215.1:c.197C>A, NM_001367846.1:c.275C>A, NM_001367848.1:c.239C>A, NM_001367843.1:c.236C>A, NM_001367845.1:c.218C>A, NM_001367847.1:c.251C>A, NM_001367842.1:c.236C>A, NM_001367850.1:c.185C>A, NM_001367844.1:c.218C>A, NM_001367851.1:c.38C>A, NM_001367852.1:c.38C>A, NM_001367849.1:c.230C>A, XP_006718357.1:p.Ala84Asp, NP_006748.1:p.Ala81Asp, XP_006718363.1:p.Ala68Asp, XP_011518645.1:p.Ala92Asp, NP_001036246.1:p.Ala79Asp, NP_001036247.1:p.Ala73Asp, NP_001036245.1:p.Ala73Asp, XP_006718362.1:p.Ala72Asp, NP_001284575.1:p.Ala73Asp, XP_016873705.1:p.Ala86Asp, NP_001350490.1:p.Ala84Asp, XP_016873695.1:p.Ala92Asp, XP_016873706.1:p.Ala79Asp, XP_016873694.1:p.Ala79Asp, XP_016873696.1:p.Ala88Asp, XP_016873707.1:p.Ala75Asp, XP_016873698.1:p.Ala80Asp, XP_024304437.1:p.Ala79Asp, XP_016873697.1:p.Ala85Asp, XP_016873708.1:p.Ala62Asp, XP_016873700.1:p.Ala75Asp, XP_016873699.1:p.Ala77Asp, XP_016873701.1:p.Ala74Asp, XP_024304438.1:p.Ala73Asp, XP_024304439.1:p.Ala72Asp, XP_016873702.1:p.Ala69Asp, XP_016873703.1:p.Ala68Asp, XP_024304440.1:p.Ala66Asp, XP_016873704.1:p.Ala66Asp, NP_001354775.1:p.Ala92Asp, NP_001354777.1:p.Ala80Asp, NP_001354772.1:p.Ala79Asp, NP_001354774.1:p.Ala73Asp, NP_001354776.1:p.Ala84Asp, NP_001354771.1:p.Ala79Asp, NP_001354779.1:p.Ala62Asp, NP_001354773.1:p.Ala73Asp, NP_001354780.1:p.Ala13Asp, NP_001354781.1:p.Ala13Asp, NP_001354778.1:p.Ala77Asp

            6.

            rs1480393765 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>G [Show Flanks]
              Chromosome:
              11:1925268 (GRCh38)
              11:1946498 (GRCh37)
              Canonical SPDI:
              NC_000011.10:1925267:A:G
              Gene:
              TNNT3 (Varview)
              Functional Consequence:
              intron_variant,coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa
              MAF:
              G=0.000071/1 (ALFA)
              G=0.000004/1 (TOPMED)
              HGVS:
              NC_000011.10:g.1925268A>G, NC_000011.9:g.1946498A>G, NW_021160004.1:g.94092A>G, XM_006718294.4:c.80A>G, XM_006718294.3:c.80A>G, XM_006718294.2:c.80A>G, XM_006718294.1:c.80A>G, XM_011520343.3:c.80A>G, XM_011520343.2:c.80A>G, XM_011520343.1:c.80A>G, NM_001042781.3:c.80A>G, NM_001042781.2:c.80A>G, XM_017018216.2:c.62A>G, XM_017018216.1:c.62A>G, NM_001363561.2:c.80A>G, NM_001363561.1:c.80A>G, XM_017018206.2:c.80A>G, XM_017018206.1:c.80A>G, XM_017018205.2:c.80A>G, XM_017018205.1:c.80A>G, XM_017018207.2:c.80A>G, XM_017018207.1:c.80A>G, XM_017018209.2:c.80A>G, XM_017018209.1:c.80A>G, XM_024448669.2:c.80A>G, XM_024448669.1:c.80A>G, XM_017018211.2:c.80A>G, XM_017018211.1:c.80A>G, XM_017018212.2:c.62A>G, XM_017018212.1:c.62A>G, XM_024448670.2:c.62A>G, XM_024448670.1:c.62A>G, XM_017018213.2:c.62A>G, XM_017018213.1:c.62A>G, NM_001367846.1:c.80A>G, NM_001367848.1:c.80A>G, NM_001367843.1:c.80A>G, NM_001367845.1:c.62A>G, NM_001367847.1:c.80A>G, NM_001367842.1:c.80A>G, NM_001367849.1:c.62A>G, XP_006718357.1:p.His27Arg, XP_011518645.1:p.His27Arg, NP_001036246.1:p.His27Arg, XP_016873705.1:p.His21Arg, NP_001350490.1:p.His27Arg, XP_016873695.1:p.His27Arg, XP_016873694.1:p.His27Arg, XP_016873696.1:p.His27Arg, XP_016873698.1:p.His27Arg, XP_024304437.1:p.His27Arg, XP_016873700.1:p.His27Arg, XP_016873701.1:p.His21Arg, XP_024304438.1:p.His21Arg, XP_016873702.1:p.His21Arg, NP_001354775.1:p.His27Arg, NP_001354777.1:p.His27Arg, NP_001354772.1:p.His27Arg, NP_001354774.1:p.His21Arg, NP_001354776.1:p.His27Arg, NP_001354771.1:p.His27Arg, NP_001354778.1:p.His21Arg

              7.

              rs1476389185 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>G [Show Flanks]
                Chromosome:
                11:1923050 (GRCh38)
                11:1944280 (GRCh37)
                Canonical SPDI:
                NC_000011.10:1923049:A:G
                Gene:
                TNNT3 (Varview)
                Functional Consequence:
                intron_variant,coding_sequence_variant,missense_variant
                HGVS:
                NC_000011.10:g.1923050A>G, NC_000011.9:g.1944280A>G, NW_021160004.1:g.91874A>G, XM_006718294.4:c.20A>G, XM_006718294.3:c.20A>G, XM_006718294.2:c.20A>G, XM_006718294.1:c.20A>G, NM_006757.4:c.20A>G, NM_006757.3:c.20A>G, XM_006718300.4:c.20A>G, XM_006718300.3:c.20A>G, XM_006718300.2:c.20A>G, XM_006718300.1:c.20A>G, XM_011520343.3:c.20A>G, XM_011520343.2:c.20A>G, XM_011520343.1:c.20A>G, NM_001042781.3:c.20A>G, NM_001042781.2:c.20A>G, NM_001042782.3:c.20A>G, NM_001042782.2:c.20A>G, NM_001042780.3:c.20A>G, NM_001042780.2:c.20A>G, XM_006718299.3:c.20A>G, XM_006718299.2:c.20A>G, XM_006718299.1:c.20A>G, NM_001297646.2:c.20A>G, NM_001297646.1:c.20A>G, XM_017018216.2:c.20A>G, XM_017018216.1:c.20A>G, NM_001363561.2:c.20A>G, NM_001363561.1:c.20A>G, XM_017018206.2:c.20A>G, XM_017018206.1:c.20A>G, XM_017018217.2:c.20A>G, XM_017018217.1:c.20A>G, XM_017018205.2:c.20A>G, XM_017018205.1:c.20A>G, XM_017018207.2:c.20A>G, XM_017018207.1:c.20A>G, XM_017018218.2:c.20A>G, XM_017018218.1:c.20A>G, XM_017018209.2:c.20A>G, XM_017018209.1:c.20A>G, XM_024448669.2:c.20A>G, XM_024448669.1:c.20A>G, XM_017018208.2:c.20A>G, XM_017018208.1:c.20A>G, XM_017018219.2:c.20A>G, XM_017018219.1:c.20A>G, XM_017018211.2:c.20A>G, XM_017018211.1:c.20A>G, XM_017018210.2:c.20A>G, XM_017018210.1:c.20A>G, XM_017018212.2:c.20A>G, XM_017018212.1:c.20A>G, XM_024448670.2:c.20A>G, XM_024448670.1:c.20A>G, XM_024448671.2:c.20A>G, XM_024448671.1:c.20A>G, XM_017018213.2:c.20A>G, XM_017018213.1:c.20A>G, XM_017018214.2:c.20A>G, XM_017018214.1:c.20A>G, XM_024448672.2:c.20A>G, XM_024448672.1:c.20A>G, XM_017018215.2:c.20A>G, XM_017018215.1:c.20A>G, NM_001367846.1:c.20A>G, NM_001367848.1:c.20A>G, NM_001367843.1:c.20A>G, NM_001367845.1:c.20A>G, NM_001367847.1:c.20A>G, NM_001367842.1:c.20A>G, NM_001367850.1:c.20A>G, NM_001367844.1:c.20A>G, NM_001367849.1:c.20A>G, XP_006718357.1:p.Glu7Gly, NP_006748.1:p.Glu7Gly, XP_006718363.1:p.Glu7Gly, XP_011518645.1:p.Glu7Gly, NP_001036246.1:p.Glu7Gly, NP_001036247.1:p.Glu7Gly, NP_001036245.1:p.Glu7Gly, XP_006718362.1:p.Glu7Gly, NP_001284575.1:p.Glu7Gly, XP_016873705.1:p.Glu7Gly, NP_001350490.1:p.Glu7Gly, XP_016873695.1:p.Glu7Gly, XP_016873706.1:p.Glu7Gly, XP_016873694.1:p.Glu7Gly, XP_016873696.1:p.Glu7Gly, XP_016873707.1:p.Glu7Gly, XP_016873698.1:p.Glu7Gly, XP_024304437.1:p.Glu7Gly, XP_016873697.1:p.Glu7Gly, XP_016873708.1:p.Glu7Gly, XP_016873700.1:p.Glu7Gly, XP_016873699.1:p.Glu7Gly, XP_016873701.1:p.Glu7Gly, XP_024304438.1:p.Glu7Gly, XP_024304439.1:p.Glu7Gly, XP_016873702.1:p.Glu7Gly, XP_016873703.1:p.Glu7Gly, XP_024304440.1:p.Glu7Gly, XP_016873704.1:p.Glu7Gly, NP_001354775.1:p.Glu7Gly, NP_001354777.1:p.Glu7Gly, NP_001354772.1:p.Glu7Gly, NP_001354774.1:p.Glu7Gly, NP_001354776.1:p.Glu7Gly, NP_001354771.1:p.Glu7Gly, NP_001354779.1:p.Glu7Gly, NP_001354773.1:p.Glu7Gly, NP_001354778.1:p.Glu7Gly

                8.

                rs1467626810 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  11:1934371 (GRCh38)
                  11:1955601 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:1934370:A:G
                  Gene:
                  TNNT3 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,missense_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  G=0.000007/1 (GnomAD)
                  HGVS:
                  NC_000011.10:g.1934371A>G, NC_000011.9:g.1955601A>G, NW_021160004.1:g.103199A>G, XM_006718294.4:c.415A>G, XM_006718294.3:c.415A>G, XM_006718294.2:c.415A>G, XM_006718294.1:c.415A>G, NM_006757.4:c.406A>G, NM_006757.3:c.406A>G, XM_006718300.4:c.367A>G, XM_006718300.3:c.367A>G, XM_006718300.2:c.367A>G, XM_006718300.1:c.367A>G, XM_011520343.3:c.439A>G, XM_011520343.2:c.439A>G, XM_011520343.1:c.439A>G, NM_001042781.3:c.400A>G, NM_001042781.2:c.400A>G, NM_001042782.3:c.382A>G, NM_001042782.2:c.382A>G, NM_001042780.3:c.382A>G, NM_001042780.2:c.382A>G, XM_006718299.3:c.379A>G, XM_006718299.2:c.379A>G, XM_006718299.1:c.379A>G, NM_001297646.2:c.382A>G, NM_001297646.1:c.382A>G, XM_017018216.2:c.421A>G, XM_017018216.1:c.421A>G, NM_001363561.2:c.415A>G, NM_001363561.1:c.415A>G, XM_017018206.2:c.439A>G, XM_017018206.1:c.439A>G, XM_017018217.2:c.400A>G, XM_017018217.1:c.400A>G, XM_017018205.2:c.400A>G, XM_017018205.1:c.400A>G, XM_017018207.2:c.427A>G, XM_017018207.1:c.427A>G, XM_017018218.2:c.388A>G, XM_017018218.1:c.388A>G, XM_017018209.2:c.403A>G, XM_017018209.1:c.403A>G, XM_024448669.2:c.400A>G, XM_024448669.1:c.400A>G, XM_017018208.2:c.418A>G, XM_017018208.1:c.418A>G, XM_017018219.2:c.349A>G, XM_017018219.1:c.349A>G, XM_017018211.2:c.388A>G, XM_017018211.1:c.388A>G, XM_017018210.2:c.394A>G, XM_017018210.1:c.394A>G, XM_017018212.2:c.385A>G, XM_017018212.1:c.385A>G, XM_024448670.2:c.382A>G, XM_024448670.1:c.382A>G, XM_024448671.2:c.379A>G, XM_024448671.1:c.379A>G, XM_017018213.2:c.370A>G, XM_017018213.1:c.370A>G, XM_017018214.2:c.367A>G, XM_017018214.1:c.367A>G, XM_024448672.2:c.361A>G, XM_024448672.1:c.361A>G, XM_017018215.2:c.361A>G, XM_017018215.1:c.361A>G, NM_001367846.1:c.439A>G, NM_001367848.1:c.403A>G, NM_001367843.1:c.400A>G, NM_001367845.1:c.382A>G, NM_001367847.1:c.415A>G, NM_001367842.1:c.400A>G, NM_001367850.1:c.349A>G, NM_001367844.1:c.382A>G, NM_001367851.1:c.202A>G, NM_001367852.1:c.202A>G, NM_001367849.1:c.394A>G, XP_006718357.1:p.Arg139Gly, NP_006748.1:p.Arg136Gly, XP_006718363.1:p.Arg123Gly, XP_011518645.1:p.Arg147Gly, NP_001036246.1:p.Arg134Gly, NP_001036247.1:p.Arg128Gly, NP_001036245.1:p.Arg128Gly, XP_006718362.1:p.Arg127Gly, NP_001284575.1:p.Arg128Gly, XP_016873705.1:p.Arg141Gly, NP_001350490.1:p.Arg139Gly, XP_016873695.1:p.Arg147Gly, XP_016873706.1:p.Arg134Gly, XP_016873694.1:p.Arg134Gly, XP_016873696.1:p.Arg143Gly, XP_016873707.1:p.Arg130Gly, XP_016873698.1:p.Arg135Gly, XP_024304437.1:p.Arg134Gly, XP_016873697.1:p.Arg140Gly, XP_016873708.1:p.Arg117Gly, XP_016873700.1:p.Arg130Gly, XP_016873699.1:p.Arg132Gly, XP_016873701.1:p.Arg129Gly, XP_024304438.1:p.Arg128Gly, XP_024304439.1:p.Arg127Gly, XP_016873702.1:p.Arg124Gly, XP_016873703.1:p.Arg123Gly, XP_024304440.1:p.Arg121Gly, XP_016873704.1:p.Arg121Gly, NP_001354775.1:p.Arg147Gly, NP_001354777.1:p.Arg135Gly, NP_001354772.1:p.Arg134Gly, NP_001354774.1:p.Arg128Gly, NP_001354776.1:p.Arg139Gly, NP_001354771.1:p.Arg134Gly, NP_001354779.1:p.Arg117Gly, NP_001354773.1:p.Arg128Gly, NP_001354780.1:p.Arg68Gly, NP_001354781.1:p.Arg68Gly, NP_001354778.1:p.Arg132Gly

                  9.

                  rs1464049185 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    11:1923559 (GRCh38)
                    11:1944789 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:1923558:G:A
                    Gene:
                    TNNT3 (Varview)
                    Functional Consequence:
                    intron_variant,synonymous_variant,coding_sequence_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    A=0./0 (ALFA)
                    A=0.000004/1 (TOPMED)
                    A=0.000007/1 (GnomAD)
                    A=0.000008/2 (GnomAD_exomes)
                    HGVS:
                    NC_000011.10:g.1923559G>A, NC_000011.9:g.1944789G>A, NW_021160004.1:g.92383G>A, XM_006718294.4:c.36G>A, XM_006718294.3:c.36G>A, XM_006718294.2:c.36G>A, XM_006718294.1:c.36G>A, NM_006757.4:c.36G>A, NM_006757.3:c.36G>A, XM_006718300.4:c.36G>A, XM_006718300.3:c.36G>A, XM_006718300.2:c.36G>A, XM_006718300.1:c.36G>A, XM_011520343.3:c.36G>A, XM_011520343.2:c.36G>A, XM_011520343.1:c.36G>A, NM_001042781.3:c.36G>A, NM_001042781.2:c.36G>A, NM_001042782.3:c.36G>A, NM_001042782.2:c.36G>A, NM_001042780.3:c.36G>A, NM_001042780.2:c.36G>A, XM_006718299.3:c.36G>A, XM_006718299.2:c.36G>A, XM_006718299.1:c.36G>A, NM_001297646.2:c.36G>A, NM_001297646.1:c.36G>A, NM_001363561.2:c.36G>A, NM_001363561.1:c.36G>A, XM_017018206.2:c.36G>A, XM_017018206.1:c.36G>A, XM_017018205.2:c.36G>A, XM_017018205.1:c.36G>A, XM_017018207.2:c.36G>A, XM_017018207.1:c.36G>A, XM_017018209.2:c.36G>A, XM_017018209.1:c.36G>A, XM_024448669.2:c.36G>A, XM_024448669.1:c.36G>A, XM_017018208.2:c.36G>A, XM_017018208.1:c.36G>A, XM_017018211.2:c.36G>A, XM_017018211.1:c.36G>A, XM_017018210.2:c.36G>A, XM_017018210.1:c.36G>A, XM_024448671.2:c.36G>A, XM_024448671.1:c.36G>A, XM_017018214.2:c.36G>A, XM_017018214.1:c.36G>A, NM_001367846.1:c.36G>A, NM_001367848.1:c.36G>A, NM_001367843.1:c.36G>A, NM_001367845.1:c.36G>A, NM_001367847.1:c.36G>A, NM_001367842.1:c.36G>A, NM_001367850.1:c.36G>A, NM_001367844.1:c.36G>A

                    10.

                    rs1457812332 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>C [Show Flanks]
                      Chromosome:
                      11:1934565 (GRCh38)
                      11:1955795 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:1934564:A:C
                      Gene:
                      TNNT3 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant
                      Validated:
                      by frequency
                      MAF:
                      C=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000011.10:g.1934565A>C, NC_000011.9:g.1955795A>C, NW_021160004.1:g.103393A>C, XM_006718294.4:c.509A>C, XM_006718294.3:c.509A>C, XM_006718294.2:c.509A>C, XM_006718294.1:c.509A>C, NM_006757.4:c.500A>C, NM_006757.3:c.500A>C, XM_006718300.4:c.461A>C, XM_006718300.3:c.461A>C, XM_006718300.2:c.461A>C, XM_006718300.1:c.461A>C, XM_011520343.3:c.533A>C, XM_011520343.2:c.533A>C, XM_011520343.1:c.533A>C, NM_001042781.3:c.494A>C, NM_001042781.2:c.494A>C, NM_001042782.3:c.476A>C, NM_001042782.2:c.476A>C, NM_001042780.3:c.476A>C, NM_001042780.2:c.476A>C, XM_006718299.3:c.473A>C, XM_006718299.2:c.473A>C, XM_006718299.1:c.473A>C, NM_001297646.2:c.476A>C, NM_001297646.1:c.476A>C, XM_017018216.2:c.515A>C, XM_017018216.1:c.515A>C, NM_001363561.2:c.509A>C, NM_001363561.1:c.509A>C, XM_017018206.2:c.533A>C, XM_017018206.1:c.533A>C, XM_017018217.2:c.494A>C, XM_017018217.1:c.494A>C, XM_017018205.2:c.494A>C, XM_017018205.1:c.494A>C, XM_017018207.2:c.521A>C, XM_017018207.1:c.521A>C, XM_017018218.2:c.482A>C, XM_017018218.1:c.482A>C, XM_017018209.2:c.497A>C, XM_017018209.1:c.497A>C, XM_024448669.2:c.494A>C, XM_024448669.1:c.494A>C, XM_017018208.2:c.512A>C, XM_017018208.1:c.512A>C, XM_017018219.2:c.443A>C, XM_017018219.1:c.443A>C, XM_017018211.2:c.482A>C, XM_017018211.1:c.482A>C, XM_017018210.2:c.488A>C, XM_017018210.1:c.488A>C, XM_017018212.2:c.479A>C, XM_017018212.1:c.479A>C, XM_024448670.2:c.476A>C, XM_024448670.1:c.476A>C, XM_024448671.2:c.473A>C, XM_024448671.1:c.473A>C, XM_017018213.2:c.464A>C, XM_017018213.1:c.464A>C, XM_017018214.2:c.461A>C, XM_017018214.1:c.461A>C, XM_024448672.2:c.455A>C, XM_024448672.1:c.455A>C, XM_017018215.2:c.455A>C, XM_017018215.1:c.455A>C, NM_001367846.1:c.533A>C, NM_001367848.1:c.497A>C, NM_001367843.1:c.494A>C, NM_001367845.1:c.476A>C, NM_001367847.1:c.509A>C, NM_001367842.1:c.494A>C, NM_001367850.1:c.443A>C, NM_001367844.1:c.476A>C, NM_001367851.1:c.296A>C, NM_001367852.1:c.296A>C, NM_001367849.1:c.488A>C, XP_006718357.1:p.Lys170Thr, NP_006748.1:p.Lys167Thr, XP_006718363.1:p.Lys154Thr, XP_011518645.1:p.Lys178Thr, NP_001036246.1:p.Lys165Thr, NP_001036247.1:p.Lys159Thr, NP_001036245.1:p.Lys159Thr, XP_006718362.1:p.Lys158Thr, NP_001284575.1:p.Lys159Thr, XP_016873705.1:p.Lys172Thr, NP_001350490.1:p.Lys170Thr, XP_016873695.1:p.Lys178Thr, XP_016873706.1:p.Lys165Thr, XP_016873694.1:p.Lys165Thr, XP_016873696.1:p.Lys174Thr, XP_016873707.1:p.Lys161Thr, XP_016873698.1:p.Lys166Thr, XP_024304437.1:p.Lys165Thr, XP_016873697.1:p.Lys171Thr, XP_016873708.1:p.Lys148Thr, XP_016873700.1:p.Lys161Thr, XP_016873699.1:p.Lys163Thr, XP_016873701.1:p.Lys160Thr, XP_024304438.1:p.Lys159Thr, XP_024304439.1:p.Lys158Thr, XP_016873702.1:p.Lys155Thr, XP_016873703.1:p.Lys154Thr, XP_024304440.1:p.Lys152Thr, XP_016873704.1:p.Lys152Thr, NP_001354775.1:p.Lys178Thr, NP_001354777.1:p.Lys166Thr, NP_001354772.1:p.Lys165Thr, NP_001354774.1:p.Lys159Thr, NP_001354776.1:p.Lys170Thr, NP_001354771.1:p.Lys165Thr, NP_001354779.1:p.Lys148Thr, NP_001354773.1:p.Lys159Thr, NP_001354780.1:p.Lys99Thr, NP_001354781.1:p.Lys99Thr, NP_001354778.1:p.Lys163Thr

                      11.

                      rs1455290682 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        11:1933974 (GRCh38)
                        11:1955204 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:1933973:C:T
                        Gene:
                        TNNT3 (Varview)
                        Functional Consequence:
                        missense_variant,coding_sequence_variant
                        Clinical significance:
                        uncertain-significance
                        Validated:
                        by frequency,by cluster
                        MAF:
                        T=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000011.10:g.1933974C>T, NC_000011.9:g.1955204C>T, NW_021160004.1:g.102802C>T, XM_006718294.4:c.341C>T, XM_006718294.3:c.341C>T, XM_006718294.2:c.341C>T, XM_006718294.1:c.341C>T, NM_006757.4:c.332C>T, NM_006757.3:c.332C>T, XM_006718300.4:c.293C>T, XM_006718300.3:c.293C>T, XM_006718300.2:c.293C>T, XM_006718300.1:c.293C>T, XM_011520343.3:c.365C>T, XM_011520343.2:c.365C>T, XM_011520343.1:c.365C>T, NM_001042781.3:c.326C>T, NM_001042781.2:c.326C>T, NM_001042782.3:c.308C>T, NM_001042782.2:c.308C>T, NM_001042780.3:c.308C>T, NM_001042780.2:c.308C>T, XM_006718299.3:c.305C>T, XM_006718299.2:c.305C>T, XM_006718299.1:c.305C>T, NM_001297646.2:c.308C>T, NM_001297646.1:c.308C>T, XM_017018216.2:c.347C>T, XM_017018216.1:c.347C>T, NM_001363561.2:c.341C>T, NM_001363561.1:c.341C>T, XM_017018206.2:c.365C>T, XM_017018206.1:c.365C>T, XM_017018217.2:c.326C>T, XM_017018217.1:c.326C>T, XM_017018205.2:c.326C>T, XM_017018205.1:c.326C>T, XM_017018207.2:c.353C>T, XM_017018207.1:c.353C>T, XM_017018218.2:c.314C>T, XM_017018218.1:c.314C>T, XM_017018209.2:c.329C>T, XM_017018209.1:c.329C>T, XM_024448669.2:c.326C>T, XM_024448669.1:c.326C>T, XM_017018208.2:c.344C>T, XM_017018208.1:c.344C>T, XM_017018219.2:c.275C>T, XM_017018219.1:c.275C>T, XM_017018211.2:c.314C>T, XM_017018211.1:c.314C>T, XM_017018210.2:c.320C>T, XM_017018210.1:c.320C>T, XM_017018212.2:c.311C>T, XM_017018212.1:c.311C>T, XM_024448670.2:c.308C>T, XM_024448670.1:c.308C>T, XM_024448671.2:c.305C>T, XM_024448671.1:c.305C>T, XM_017018213.2:c.296C>T, XM_017018213.1:c.296C>T, XM_017018214.2:c.293C>T, XM_017018214.1:c.293C>T, XM_024448672.2:c.287C>T, XM_024448672.1:c.287C>T, XM_017018215.2:c.287C>T, XM_017018215.1:c.287C>T, NM_001367846.1:c.365C>T, NM_001367848.1:c.329C>T, NM_001367843.1:c.326C>T, NM_001367845.1:c.308C>T, NM_001367847.1:c.341C>T, NM_001367842.1:c.326C>T, NM_001367850.1:c.275C>T, NM_001367844.1:c.308C>T, NM_001367851.1:c.128C>T, NM_001367852.1:c.128C>T, NM_001367849.1:c.320C>T, XP_006718357.1:p.Ala114Val, NP_006748.1:p.Ala111Val, XP_006718363.1:p.Ala98Val, XP_011518645.1:p.Ala122Val, NP_001036246.1:p.Ala109Val, NP_001036247.1:p.Ala103Val, NP_001036245.1:p.Ala103Val, XP_006718362.1:p.Ala102Val, NP_001284575.1:p.Ala103Val, XP_016873705.1:p.Ala116Val, NP_001350490.1:p.Ala114Val, XP_016873695.1:p.Ala122Val, XP_016873706.1:p.Ala109Val, XP_016873694.1:p.Ala109Val, XP_016873696.1:p.Ala118Val, XP_016873707.1:p.Ala105Val, XP_016873698.1:p.Ala110Val, XP_024304437.1:p.Ala109Val, XP_016873697.1:p.Ala115Val, XP_016873708.1:p.Ala92Val, XP_016873700.1:p.Ala105Val, XP_016873699.1:p.Ala107Val, XP_016873701.1:p.Ala104Val, XP_024304438.1:p.Ala103Val, XP_024304439.1:p.Ala102Val, XP_016873702.1:p.Ala99Val, XP_016873703.1:p.Ala98Val, XP_024304440.1:p.Ala96Val, XP_016873704.1:p.Ala96Val, NP_001354775.1:p.Ala122Val, NP_001354777.1:p.Ala110Val, NP_001354772.1:p.Ala109Val, NP_001354774.1:p.Ala103Val, NP_001354776.1:p.Ala114Val, NP_001354771.1:p.Ala109Val, NP_001354779.1:p.Ala92Val, NP_001354773.1:p.Ala103Val, NP_001354780.1:p.Ala43Val, NP_001354781.1:p.Ala43Val, NP_001354778.1:p.Ala107Val

                        12.

                        rs1450304341 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          11:1934358 (GRCh38)
                          11:1955588 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:1934357:G:A
                          Gene:
                          TNNT3 (Varview)
                          Functional Consequence:
                          synonymous_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000007/1 (GnomAD)
                          HGVS:
                          NC_000011.10:g.1934358G>A, NC_000011.9:g.1955588G>A, NW_021160004.1:g.103186G>A, XM_006718294.4:c.402G>A, XM_006718294.3:c.402G>A, XM_006718294.2:c.402G>A, XM_006718294.1:c.402G>A, NM_006757.4:c.393G>A, NM_006757.3:c.393G>A, XM_006718300.4:c.354G>A, XM_006718300.3:c.354G>A, XM_006718300.2:c.354G>A, XM_006718300.1:c.354G>A, XM_011520343.3:c.426G>A, XM_011520343.2:c.426G>A, XM_011520343.1:c.426G>A, NM_001042781.3:c.387G>A, NM_001042781.2:c.387G>A, NM_001042782.3:c.369G>A, NM_001042782.2:c.369G>A, NM_001042780.3:c.369G>A, NM_001042780.2:c.369G>A, XM_006718299.3:c.366G>A, XM_006718299.2:c.366G>A, XM_006718299.1:c.366G>A, NM_001297646.2:c.369G>A, NM_001297646.1:c.369G>A, XM_017018216.2:c.408G>A, XM_017018216.1:c.408G>A, NM_001363561.2:c.402G>A, NM_001363561.1:c.402G>A, XM_017018206.2:c.426G>A, XM_017018206.1:c.426G>A, XM_017018217.2:c.387G>A, XM_017018217.1:c.387G>A, XM_017018205.2:c.387G>A, XM_017018205.1:c.387G>A, XM_017018207.2:c.414G>A, XM_017018207.1:c.414G>A, XM_017018218.2:c.375G>A, XM_017018218.1:c.375G>A, XM_017018209.2:c.390G>A, XM_017018209.1:c.390G>A, XM_024448669.2:c.387G>A, XM_024448669.1:c.387G>A, XM_017018208.2:c.405G>A, XM_017018208.1:c.405G>A, XM_017018219.2:c.336G>A, XM_017018219.1:c.336G>A, XM_017018211.2:c.375G>A, XM_017018211.1:c.375G>A, XM_017018210.2:c.381G>A, XM_017018210.1:c.381G>A, XM_017018212.2:c.372G>A, XM_017018212.1:c.372G>A, XM_024448670.2:c.369G>A, XM_024448670.1:c.369G>A, XM_024448671.2:c.366G>A, XM_024448671.1:c.366G>A, XM_017018213.2:c.357G>A, XM_017018213.1:c.357G>A, XM_017018214.2:c.354G>A, XM_017018214.1:c.354G>A, XM_024448672.2:c.348G>A, XM_024448672.1:c.348G>A, XM_017018215.2:c.348G>A, XM_017018215.1:c.348G>A, NM_001367846.1:c.426G>A, NM_001367848.1:c.390G>A, NM_001367843.1:c.387G>A, NM_001367845.1:c.369G>A, NM_001367847.1:c.402G>A, NM_001367842.1:c.387G>A, NM_001367850.1:c.336G>A, NM_001367844.1:c.369G>A, NM_001367851.1:c.189G>A, NM_001367852.1:c.189G>A, NM_001367849.1:c.381G>A

                          13.

                          rs1442586573 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A [Show Flanks]
                            Chromosome:
                            11:1932488 (GRCh38)
                            11:1953718 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:1932487:C:A
                            Gene:
                            TNNT3 (Varview)
                            Functional Consequence:
                            5_prime_UTR_variant,coding_sequence_variant,missense_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000007/1 (GnomAD)
                            HGVS:
                            NC_000011.10:g.1932488C>A, NC_000011.9:g.1953718C>A, NW_021160004.1:g.101310C>A, XM_006718294.4:c.154C>A, XM_006718294.3:c.154C>A, XM_006718294.2:c.154C>A, XM_006718294.1:c.154C>A, NM_006757.4:c.145C>A, NM_006757.3:c.145C>A, XM_006718300.4:c.106C>A, XM_006718300.3:c.106C>A, XM_006718300.2:c.106C>A, XM_006718300.1:c.106C>A, XM_011520343.3:c.178C>A, XM_011520343.2:c.178C>A, XM_011520343.1:c.178C>A, NM_001042781.3:c.139C>A, NM_001042781.2:c.139C>A, NM_001042782.3:c.121C>A, NM_001042782.2:c.121C>A, NM_001042780.3:c.121C>A, NM_001042780.2:c.121C>A, XM_006718299.3:c.118C>A, XM_006718299.2:c.118C>A, XM_006718299.1:c.118C>A, NM_001297646.2:c.121C>A, NM_001297646.1:c.121C>A, XM_017018216.2:c.160C>A, XM_017018216.1:c.160C>A, NM_001363561.2:c.154C>A, NM_001363561.1:c.154C>A, XM_017018206.2:c.178C>A, XM_017018206.1:c.178C>A, XM_017018217.2:c.139C>A, XM_017018217.1:c.139C>A, XM_017018205.2:c.139C>A, XM_017018205.1:c.139C>A, XM_017018207.2:c.166C>A, XM_017018207.1:c.166C>A, XM_017018218.2:c.127C>A, XM_017018218.1:c.127C>A, XM_017018209.2:c.142C>A, XM_017018209.1:c.142C>A, XM_024448669.2:c.139C>A, XM_024448669.1:c.139C>A, XM_017018208.2:c.157C>A, XM_017018208.1:c.157C>A, XM_017018219.2:c.88C>A, XM_017018219.1:c.88C>A, XM_017018211.2:c.127C>A, XM_017018211.1:c.127C>A, XM_017018210.2:c.133C>A, XM_017018210.1:c.133C>A, XM_017018212.2:c.124C>A, XM_017018212.1:c.124C>A, XM_024448670.2:c.121C>A, XM_024448670.1:c.121C>A, XM_024448671.2:c.118C>A, XM_024448671.1:c.118C>A, XM_017018213.2:c.109C>A, XM_017018213.1:c.109C>A, XM_017018214.2:c.106C>A, XM_017018214.1:c.106C>A, XM_024448672.2:c.100C>A, XM_024448672.1:c.100C>A, XM_017018215.2:c.100C>A, XM_017018215.1:c.100C>A, NM_001367846.1:c.178C>A, NM_001367848.1:c.142C>A, NM_001367843.1:c.139C>A, NM_001367845.1:c.121C>A, NM_001367847.1:c.154C>A, NM_001367842.1:c.139C>A, NM_001367850.1:c.88C>A, NM_001367844.1:c.121C>A, NM_001367851.1:c.-60C>A, NM_001367852.1:c.-60C>A, NM_001367849.1:c.133C>A, XP_006718357.1:p.Pro52Thr, NP_006748.1:p.Pro49Thr, XP_006718363.1:p.Pro36Thr, XP_011518645.1:p.Pro60Thr, NP_001036246.1:p.Pro47Thr, NP_001036247.1:p.Pro41Thr, NP_001036245.1:p.Pro41Thr, XP_006718362.1:p.Pro40Thr, NP_001284575.1:p.Pro41Thr, XP_016873705.1:p.Pro54Thr, NP_001350490.1:p.Pro52Thr, XP_016873695.1:p.Pro60Thr, XP_016873706.1:p.Pro47Thr, XP_016873694.1:p.Pro47Thr, XP_016873696.1:p.Pro56Thr, XP_016873707.1:p.Pro43Thr, XP_016873698.1:p.Pro48Thr, XP_024304437.1:p.Pro47Thr, XP_016873697.1:p.Pro53Thr, XP_016873708.1:p.Pro30Thr, XP_016873700.1:p.Pro43Thr, XP_016873699.1:p.Pro45Thr, XP_016873701.1:p.Pro42Thr, XP_024304438.1:p.Pro41Thr, XP_024304439.1:p.Pro40Thr, XP_016873702.1:p.Pro37Thr, XP_016873703.1:p.Pro36Thr, XP_024304440.1:p.Pro34Thr, XP_016873704.1:p.Pro34Thr, NP_001354775.1:p.Pro60Thr, NP_001354777.1:p.Pro48Thr, NP_001354772.1:p.Pro47Thr, NP_001354774.1:p.Pro41Thr, NP_001354776.1:p.Pro52Thr, NP_001354771.1:p.Pro47Thr, NP_001354779.1:p.Pro30Thr, NP_001354773.1:p.Pro41Thr, NP_001354778.1:p.Pro45Thr

                            14.

                            rs1442552605 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>T [Show Flanks]
                              Chromosome:
                              11:1934883 (GRCh38)
                              11:1956113 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:1934882:C:T
                              Gene:
                              TNNT3 (Varview)
                              Functional Consequence:
                              synonymous_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0.000056/2 (ALFA)
                              T=0.000008/2 (TOPMED)
                              C=0.5/1 (SGDP_PRJ)
                              HGVS:
                              NC_000011.10:g.1934883C>T, NC_000011.9:g.1956113C>T, NW_021160004.1:g.103711C>T, XM_006718294.4:c.654C>T, XM_006718294.3:c.654C>T, XM_006718294.2:c.654C>T, XM_006718294.1:c.654C>T, NM_006757.4:c.645C>T, NM_006757.3:c.645C>T, XM_006718300.4:c.606C>T, XM_006718300.3:c.606C>T, XM_006718300.2:c.606C>T, XM_006718300.1:c.606C>T, XM_011520343.3:c.678C>T, XM_011520343.2:c.678C>T, XM_011520343.1:c.678C>T, NM_001042781.3:c.639C>T, NM_001042781.2:c.639C>T, NM_001042782.3:c.621C>T, NM_001042782.2:c.621C>T, NM_001042780.3:c.621C>T, NM_001042780.2:c.621C>T, XM_006718299.3:c.618C>T, XM_006718299.2:c.618C>T, XM_006718299.1:c.618C>T, NM_001297646.2:c.621C>T, NM_001297646.1:c.621C>T, XM_017018216.2:c.660C>T, XM_017018216.1:c.660C>T, NM_001363561.2:c.654C>T, NM_001363561.1:c.654C>T, XM_017018206.2:c.678C>T, XM_017018206.1:c.678C>T, XM_017018217.2:c.639C>T, XM_017018217.1:c.639C>T, XM_017018205.2:c.639C>T, XM_017018205.1:c.639C>T, XM_017018207.2:c.666C>T, XM_017018207.1:c.666C>T, XM_017018218.2:c.627C>T, XM_017018218.1:c.627C>T, XM_017018209.2:c.642C>T, XM_017018209.1:c.642C>T, XM_024448669.2:c.639C>T, XM_024448669.1:c.639C>T, XM_017018208.2:c.657C>T, XM_017018208.1:c.657C>T, XM_017018219.2:c.588C>T, XM_017018219.1:c.588C>T, XM_017018211.2:c.627C>T, XM_017018211.1:c.627C>T, XM_017018210.2:c.633C>T, XM_017018210.1:c.633C>T, XM_017018212.2:c.624C>T, XM_017018212.1:c.624C>T, XM_024448670.2:c.621C>T, XM_024448670.1:c.621C>T, XM_024448671.2:c.618C>T, XM_024448671.1:c.618C>T, XM_017018213.2:c.609C>T, XM_017018213.1:c.609C>T, XM_017018214.2:c.606C>T, XM_017018214.1:c.606C>T, XM_024448672.2:c.600C>T, XM_024448672.1:c.600C>T, XM_017018215.2:c.600C>T, XM_017018215.1:c.600C>T, NM_001367846.1:c.678C>T, NM_001367848.1:c.642C>T, NM_001367843.1:c.639C>T, NM_001367845.1:c.621C>T, NM_001367847.1:c.654C>T, NM_001367842.1:c.639C>T, NM_001367850.1:c.588C>T, NM_001367844.1:c.621C>T, NM_001367851.1:c.441C>T, NM_001367852.1:c.441C>T, NM_001367849.1:c.633C>T

                              15.

                              rs1442420279 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                11:1934655 (GRCh38)
                                11:1955885 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:1934654:G:A
                                Gene:
                                TNNT3 (Varview)
                                Functional Consequence:
                                missense_variant,coding_sequence_variant
                                Validated:
                                by frequency
                                MAF:
                                A=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000011.10:g.1934655G>A, NC_000011.9:g.1955885G>A, NW_021160004.1:g.103483G>A, XM_006718294.4:c.599G>A, XM_006718294.3:c.599G>A, XM_006718294.2:c.599G>A, XM_006718294.1:c.599G>A, NM_006757.4:c.590G>A, NM_006757.3:c.590G>A, XM_006718300.4:c.551G>A, XM_006718300.3:c.551G>A, XM_006718300.2:c.551G>A, XM_006718300.1:c.551G>A, XM_011520343.3:c.623G>A, XM_011520343.2:c.623G>A, XM_011520343.1:c.623G>A, NM_001042781.3:c.584G>A, NM_001042781.2:c.584G>A, NM_001042782.3:c.566G>A, NM_001042782.2:c.566G>A, NM_001042780.3:c.566G>A, NM_001042780.2:c.566G>A, XM_006718299.3:c.563G>A, XM_006718299.2:c.563G>A, XM_006718299.1:c.563G>A, NM_001297646.2:c.566G>A, NM_001297646.1:c.566G>A, XM_017018216.2:c.605G>A, XM_017018216.1:c.605G>A, NM_001363561.2:c.599G>A, NM_001363561.1:c.599G>A, XM_017018206.2:c.623G>A, XM_017018206.1:c.623G>A, XM_017018217.2:c.584G>A, XM_017018217.1:c.584G>A, XM_017018205.2:c.584G>A, XM_017018205.1:c.584G>A, XM_017018207.2:c.611G>A, XM_017018207.1:c.611G>A, XM_017018218.2:c.572G>A, XM_017018218.1:c.572G>A, XM_017018209.2:c.587G>A, XM_017018209.1:c.587G>A, XM_024448669.2:c.584G>A, XM_024448669.1:c.584G>A, XM_017018208.2:c.602G>A, XM_017018208.1:c.602G>A, XM_017018219.2:c.533G>A, XM_017018219.1:c.533G>A, XM_017018211.2:c.572G>A, XM_017018211.1:c.572G>A, XM_017018210.2:c.578G>A, XM_017018210.1:c.578G>A, XM_017018212.2:c.569G>A, XM_017018212.1:c.569G>A, XM_024448670.2:c.566G>A, XM_024448670.1:c.566G>A, XM_024448671.2:c.563G>A, XM_024448671.1:c.563G>A, XM_017018213.2:c.554G>A, XM_017018213.1:c.554G>A, XM_017018214.2:c.551G>A, XM_017018214.1:c.551G>A, XM_024448672.2:c.545G>A, XM_024448672.1:c.545G>A, XM_017018215.2:c.545G>A, XM_017018215.1:c.545G>A, NM_001367846.1:c.623G>A, NM_001367848.1:c.587G>A, NM_001367843.1:c.584G>A, NM_001367845.1:c.566G>A, NM_001367847.1:c.599G>A, NM_001367842.1:c.584G>A, NM_001367850.1:c.533G>A, NM_001367844.1:c.566G>A, NM_001367851.1:c.386G>A, NM_001367852.1:c.386G>A, NM_001367849.1:c.578G>A, XP_006718357.1:p.Arg200Lys, NP_006748.1:p.Arg197Lys, XP_006718363.1:p.Arg184Lys, XP_011518645.1:p.Arg208Lys, NP_001036246.1:p.Arg195Lys, NP_001036247.1:p.Arg189Lys, NP_001036245.1:p.Arg189Lys, XP_006718362.1:p.Arg188Lys, NP_001284575.1:p.Arg189Lys, XP_016873705.1:p.Arg202Lys, NP_001350490.1:p.Arg200Lys, XP_016873695.1:p.Arg208Lys, XP_016873706.1:p.Arg195Lys, XP_016873694.1:p.Arg195Lys, XP_016873696.1:p.Arg204Lys, XP_016873707.1:p.Arg191Lys, XP_016873698.1:p.Arg196Lys, XP_024304437.1:p.Arg195Lys, XP_016873697.1:p.Arg201Lys, XP_016873708.1:p.Arg178Lys, XP_016873700.1:p.Arg191Lys, XP_016873699.1:p.Arg193Lys, XP_016873701.1:p.Arg190Lys, XP_024304438.1:p.Arg189Lys, XP_024304439.1:p.Arg188Lys, XP_016873702.1:p.Arg185Lys, XP_016873703.1:p.Arg184Lys, XP_024304440.1:p.Arg182Lys, XP_016873704.1:p.Arg182Lys, NP_001354775.1:p.Arg208Lys, NP_001354777.1:p.Arg196Lys, NP_001354772.1:p.Arg195Lys, NP_001354774.1:p.Arg189Lys, NP_001354776.1:p.Arg200Lys, NP_001354771.1:p.Arg195Lys, NP_001354779.1:p.Arg178Lys, NP_001354773.1:p.Arg189Lys, NP_001354780.1:p.Arg129Lys, NP_001354781.1:p.Arg129Lys, NP_001354778.1:p.Arg193Lys

                                16.

                                rs1435275589 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  AAG>- [Show Flanks]
                                  Chromosome:
                                  11:1933979 (GRCh38)
                                  11:1955209 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:1933976:AGAAG:AG
                                  Gene:
                                  TNNT3 (Varview)
                                  Functional Consequence:
                                  inframe_deletion,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  AG=0./0 (ALFA)
                                  -=0.000007/1 (GnomAD)
                                  -=0.000008/2 (TOPMED)
                                  HGVS:
                                  NC_000011.10:g.1933979_1933981del, NC_000011.9:g.1955209_1955211del, NW_021160004.1:g.102807_102809del, XM_006718294.4:c.346_348del, XM_006718294.3:c.346_348del, XM_006718294.2:c.346_348del, XM_006718294.1:c.346_348del, NM_006757.4:c.337_339del, NM_006757.3:c.337_339del, XM_006718300.4:c.298_300del, XM_006718300.3:c.298_300del, XM_006718300.2:c.298_300del, XM_006718300.1:c.298_300del, XM_011520343.3:c.370_372del, XM_011520343.2:c.370_372del, XM_011520343.1:c.370_372del, NM_001042781.3:c.331_333del, NM_001042781.2:c.331_333del, NM_001042782.3:c.313_315del, NM_001042782.2:c.313_315del, NM_001042780.3:c.313_315del, NM_001042780.2:c.313_315del, XM_006718299.3:c.310_312del, XM_006718299.2:c.310_312del, XM_006718299.1:c.310_312del, NM_001297646.2:c.313_315del, NM_001297646.1:c.313_315del, XM_017018216.2:c.352_354del, XM_017018216.1:c.352_354del, NM_001363561.2:c.346_348del, NM_001363561.1:c.346_348del, XM_017018206.2:c.370_372del, XM_017018206.1:c.370_372del, XM_017018217.2:c.331_333del, XM_017018217.1:c.331_333del, XM_017018205.2:c.331_333del, XM_017018205.1:c.331_333del, XM_017018207.2:c.358_360del, XM_017018207.1:c.358_360del, XM_017018218.2:c.319_321del, XM_017018218.1:c.319_321del, XM_017018209.2:c.334_336del, XM_017018209.1:c.334_336del, XM_024448669.2:c.331_333del, XM_024448669.1:c.331_333del, XM_017018208.2:c.349_351del, XM_017018208.1:c.349_351del, XM_017018219.2:c.280_282del, XM_017018219.1:c.280_282del, XM_017018211.2:c.319_321del, XM_017018211.1:c.319_321del, XM_017018210.2:c.325_327del, XM_017018210.1:c.325_327del, XM_017018212.2:c.316_318del, XM_017018212.1:c.316_318del, XM_024448670.2:c.313_315del, XM_024448670.1:c.313_315del, XM_024448671.2:c.310_312del, XM_024448671.1:c.310_312del, XM_017018213.2:c.301_303del, XM_017018213.1:c.301_303del, XM_017018214.2:c.298_300del, XM_017018214.1:c.298_300del, XM_024448672.2:c.292_294del, XM_024448672.1:c.292_294del, XM_017018215.2:c.292_294del, XM_017018215.1:c.292_294del, NM_001367846.1:c.370_372del, NM_001367848.1:c.334_336del, NM_001367843.1:c.331_333del, NM_001367845.1:c.313_315del, NM_001367847.1:c.346_348del, NM_001367842.1:c.331_333del, NM_001367850.1:c.280_282del, NM_001367844.1:c.313_315del, NM_001367851.1:c.133_135del, NM_001367852.1:c.133_135del, NM_001367849.1:c.325_327del, XP_006718357.1:p.Lys116del, NP_006748.1:p.Lys113del, XP_006718363.1:p.Lys100del, XP_011518645.1:p.Lys124del, NP_001036246.1:p.Lys111del, NP_001036247.1:p.Lys105del, NP_001036245.1:p.Lys105del, XP_006718362.1:p.Lys104del, NP_001284575.1:p.Lys105del, XP_016873705.1:p.Lys118del, NP_001350490.1:p.Lys116del, XP_016873695.1:p.Lys124del, XP_016873706.1:p.Lys111del, XP_016873694.1:p.Lys111del, XP_016873696.1:p.Lys120del, XP_016873707.1:p.Lys107del, XP_016873698.1:p.Lys112del, XP_024304437.1:p.Lys111del, XP_016873697.1:p.Lys117del, XP_016873708.1:p.Lys94del, XP_016873700.1:p.Lys107del, XP_016873699.1:p.Lys109del, XP_016873701.1:p.Lys106del, XP_024304438.1:p.Lys105del, XP_024304439.1:p.Lys104del, XP_016873702.1:p.Lys101del, XP_016873703.1:p.Lys100del, XP_024304440.1:p.Lys98del, XP_016873704.1:p.Lys98del, NP_001354775.1:p.Lys124del, NP_001354777.1:p.Lys112del, NP_001354772.1:p.Lys111del, NP_001354774.1:p.Lys105del, NP_001354776.1:p.Lys116del, NP_001354771.1:p.Lys111del, NP_001354779.1:p.Lys94del, NP_001354773.1:p.Lys105del, NP_001354780.1:p.Lys45del, NP_001354781.1:p.Lys45del, NP_001354778.1:p.Lys109del

                                  17.

                                  rs1426206593 has merged into rs765275660 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    AGA>-,AGAAGA [Show Flanks]
                                    Chromosome:
                                    11:1934595 (GRCh38)
                                    11:1955825 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:1934586:GAAGAAGAAGA:GAAGAAGA,NC_000011.10:1934586:GAAGAAGAAGA:GAAGAAGAAGAAGA
                                    Gene:
                                    TNNT3 (Varview)
                                    Functional Consequence:
                                    inframe_deletion,coding_sequence_variant,inframe_insertion
                                    Clinical significance:
                                    uncertain-significance
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    GAAGAAGA=0.000109/3 (ALFA)
                                    -=0.000021/3 (GnomAD)
                                    -=0.000035/1 (TOMMO)
                                    -=0.000041/4 (ExAC)
                                    -=0.000045/11 (GnomAD_exomes)
                                    -=0.000223/1 (Estonian)
                                    HGVS:
                                    NC_000011.10:g.1934589AGA[2], NC_000011.10:g.1934589AGA[4], NC_000011.9:g.1955819AGA[2], NC_000011.9:g.1955819AGA[4], NW_021160004.1:g.103417AGA[2], NW_021160004.1:g.103417AGA[4], XM_006718294.4:c.533AGA[2], XM_006718294.4:c.533AGA[4], XM_006718294.3:c.533AGA[2], XM_006718294.3:c.533AGA[4], XM_006718294.2:c.533AGA[2], XM_006718294.2:c.533AGA[4], XM_006718294.1:c.533AGA[2], XM_006718294.1:c.533AGA[4], NM_006757.4:c.524AGA[2], NM_006757.4:c.524AGA[4], NM_006757.3:c.524AGA[2], NM_006757.3:c.524AGA[4], XM_006718300.4:c.485AGA[2], XM_006718300.4:c.485AGA[4], XM_006718300.3:c.485AGA[2], XM_006718300.3:c.485AGA[4], XM_006718300.2:c.485AGA[2], XM_006718300.2:c.485AGA[4], XM_006718300.1:c.485AGA[2], XM_006718300.1:c.485AGA[4], XM_011520343.3:c.557AGA[2], XM_011520343.3:c.557AGA[4], XM_011520343.2:c.557AGA[2], XM_011520343.2:c.557AGA[4], XM_011520343.1:c.557AGA[2], XM_011520343.1:c.557AGA[4], NM_001042781.3:c.518AGA[2], NM_001042781.3:c.518AGA[4], NM_001042781.2:c.518AGA[2], NM_001042781.2:c.518AGA[4], NM_001042782.3:c.500AGA[2], NM_001042782.3:c.500AGA[4], NM_001042782.2:c.500AGA[2], NM_001042782.2:c.500AGA[4], NM_001042780.3:c.500AGA[2], NM_001042780.3:c.500AGA[4], NM_001042780.2:c.500AGA[2], NM_001042780.2:c.500AGA[4], XM_006718299.3:c.497AGA[2], XM_006718299.3:c.497AGA[4], XM_006718299.2:c.497AGA[2], XM_006718299.2:c.497AGA[4], XM_006718299.1:c.497AGA[2], XM_006718299.1:c.497AGA[4], NM_001297646.2:c.500AGA[2], NM_001297646.2:c.500AGA[4], NM_001297646.1:c.500AGA[2], NM_001297646.1:c.500AGA[4], XM_017018216.2:c.539AGA[2], XM_017018216.2:c.539AGA[4], XM_017018216.1:c.539AGA[2], XM_017018216.1:c.539AGA[4], NM_001363561.2:c.533AGA[2], NM_001363561.2:c.533AGA[4], NM_001363561.1:c.533AGA[2], NM_001363561.1:c.533AGA[4], XM_017018206.2:c.557AGA[2], XM_017018206.2:c.557AGA[4], XM_017018206.1:c.557AGA[2], XM_017018206.1:c.557AGA[4], XM_017018217.2:c.518AGA[2], XM_017018217.2:c.518AGA[4], XM_017018217.1:c.518AGA[2], XM_017018217.1:c.518AGA[4], XM_017018205.2:c.518AGA[2], XM_017018205.2:c.518AGA[4], XM_017018205.1:c.518AGA[2], XM_017018205.1:c.518AGA[4], XM_017018207.2:c.545AGA[2], XM_017018207.2:c.545AGA[4], XM_017018207.1:c.545AGA[2], XM_017018207.1:c.545AGA[4], XM_017018218.2:c.506AGA[2], XM_017018218.2:c.506AGA[4], XM_017018218.1:c.506AGA[2], XM_017018218.1:c.506AGA[4], XM_017018209.2:c.521AGA[2], XM_017018209.2:c.521AGA[4], XM_017018209.1:c.521AGA[2], XM_017018209.1:c.521AGA[4], XM_024448669.2:c.518AGA[2], XM_024448669.2:c.518AGA[4], XM_024448669.1:c.518AGA[2], XM_024448669.1:c.518AGA[4], XM_017018208.2:c.536AGA[2], XM_017018208.2:c.536AGA[4], XM_017018208.1:c.536AGA[2], XM_017018208.1:c.536AGA[4], XM_017018219.2:c.467AGA[2], XM_017018219.2:c.467AGA[4], XM_017018219.1:c.467AGA[2], XM_017018219.1:c.467AGA[4], XM_017018211.2:c.506AGA[2], XM_017018211.2:c.506AGA[4], XM_017018211.1:c.506AGA[2], XM_017018211.1:c.506AGA[4], XM_017018210.2:c.512AGA[2], XM_017018210.2:c.512AGA[4], XM_017018210.1:c.512AGA[2], XM_017018210.1:c.512AGA[4], XM_017018212.2:c.503AGA[2], XM_017018212.2:c.503AGA[4], XM_017018212.1:c.503AGA[2], XM_017018212.1:c.503AGA[4], XM_024448670.2:c.500AGA[2], XM_024448670.2:c.500AGA[4], XM_024448670.1:c.500AGA[2], XM_024448670.1:c.500AGA[4], XM_024448671.2:c.497AGA[2], XM_024448671.2:c.497AGA[4], XM_024448671.1:c.497AGA[2], XM_024448671.1:c.497AGA[4], XM_017018213.2:c.488AGA[2], XM_017018213.2:c.488AGA[4], XM_017018213.1:c.488AGA[2], XM_017018213.1:c.488AGA[4], XM_017018214.2:c.485AGA[2], XM_017018214.2:c.485AGA[4], XM_017018214.1:c.485AGA[2], XM_017018214.1:c.485AGA[4], XM_024448672.2:c.479AGA[2], XM_024448672.2:c.479AGA[4], XM_024448672.1:c.479AGA[2], XM_024448672.1:c.479AGA[4], XM_017018215.2:c.479AGA[2], XM_017018215.2:c.479AGA[4], XM_017018215.1:c.479AGA[2], XM_017018215.1:c.479AGA[4], NM_001367846.1:c.557AGA[2], NM_001367846.1:c.557AGA[4], NM_001367848.1:c.521AGA[2], NM_001367848.1:c.521AGA[4], NM_001367843.1:c.518AGA[2], NM_001367843.1:c.518AGA[4], NM_001367845.1:c.500AGA[2], NM_001367845.1:c.500AGA[4], NM_001367847.1:c.533AGA[2], NM_001367847.1:c.533AGA[4], NM_001367842.1:c.518AGA[2], NM_001367842.1:c.518AGA[4], NM_001367850.1:c.467AGA[2], NM_001367850.1:c.467AGA[4], NM_001367844.1:c.500AGA[2], NM_001367844.1:c.500AGA[4], NM_001367851.1:c.320AGA[2], NM_001367851.1:c.320AGA[4], NM_001367852.1:c.320AGA[2], NM_001367852.1:c.320AGA[4], NM_001367849.1:c.512AGA[2], NM_001367849.1:c.512AGA[4], XP_006718357.1:p.Lys180del, XP_006718357.1:p.Lys180dup, NP_006748.1:p.Lys177del, NP_006748.1:p.Lys177dup, XP_006718363.1:p.Lys164del, XP_006718363.1:p.Lys164dup, XP_011518645.1:p.Lys188del, XP_011518645.1:p.Lys188dup, NP_001036246.1:p.Lys175del, NP_001036246.1:p.Lys175dup, NP_001036247.1:p.Lys169del, NP_001036247.1:p.Lys169dup, NP_001036245.1:p.Lys169del, NP_001036245.1:p.Lys169dup, XP_006718362.1:p.Lys168del, XP_006718362.1:p.Lys168dup, NP_001284575.1:p.Lys169del, NP_001284575.1:p.Lys169dup, XP_016873705.1:p.Lys182del, XP_016873705.1:p.Lys182dup, NP_001350490.1:p.Lys180del, NP_001350490.1:p.Lys180dup, XP_016873695.1:p.Lys188del, XP_016873695.1:p.Lys188dup, XP_016873706.1:p.Lys175del, XP_016873706.1:p.Lys175dup, XP_016873694.1:p.Lys175del, XP_016873694.1:p.Lys175dup, XP_016873696.1:p.Lys184del, XP_016873696.1:p.Lys184dup, XP_016873707.1:p.Lys171del, XP_016873707.1:p.Lys171dup, XP_016873698.1:p.Lys176del, XP_016873698.1:p.Lys176dup, XP_024304437.1:p.Lys175del, XP_024304437.1:p.Lys175dup, XP_016873697.1:p.Lys181del, XP_016873697.1:p.Lys181dup, XP_016873708.1:p.Lys158del, XP_016873708.1:p.Lys158dup, XP_016873700.1:p.Lys171del, XP_016873700.1:p.Lys171dup, XP_016873699.1:p.Lys173del, XP_016873699.1:p.Lys173dup, XP_016873701.1:p.Lys170del, XP_016873701.1:p.Lys170dup, XP_024304438.1:p.Lys169del, XP_024304438.1:p.Lys169dup, XP_024304439.1:p.Lys168del, XP_024304439.1:p.Lys168dup, XP_016873702.1:p.Lys165del, XP_016873702.1:p.Lys165dup, XP_016873703.1:p.Lys164del, XP_016873703.1:p.Lys164dup, XP_024304440.1:p.Lys162del, XP_024304440.1:p.Lys162dup, XP_016873704.1:p.Lys162del, XP_016873704.1:p.Lys162dup, NP_001354775.1:p.Lys188del, NP_001354775.1:p.Lys188dup, NP_001354777.1:p.Lys176del, NP_001354777.1:p.Lys176dup, NP_001354772.1:p.Lys175del, NP_001354772.1:p.Lys175dup, NP_001354774.1:p.Lys169del, NP_001354774.1:p.Lys169dup, NP_001354776.1:p.Lys180del, NP_001354776.1:p.Lys180dup, NP_001354771.1:p.Lys175del, NP_001354771.1:p.Lys175dup, NP_001354779.1:p.Lys158del, NP_001354779.1:p.Lys158dup, NP_001354773.1:p.Lys169del, NP_001354773.1:p.Lys169dup, NP_001354780.1:p.Lys109del, NP_001354780.1:p.Lys109dup, NP_001354781.1:p.Lys109del, NP_001354781.1:p.Lys109dup, NP_001354778.1:p.Lys173del, NP_001354778.1:p.Lys173dup

                                    18.

                                    rs1424952733 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      11:1934855 (GRCh38)
                                      11:1956085 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:1934854:C:T
                                      Gene:
                                      TNNT3 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      T=0.000004/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000011.10:g.1934855C>T, NC_000011.9:g.1956085C>T, NW_021160004.1:g.103683C>T, XM_006718294.4:c.626C>T, XM_006718294.3:c.626C>T, XM_006718294.2:c.626C>T, XM_006718294.1:c.626C>T, NM_006757.4:c.617C>T, NM_006757.3:c.617C>T, XM_006718300.4:c.578C>T, XM_006718300.3:c.578C>T, XM_006718300.2:c.578C>T, XM_006718300.1:c.578C>T, XM_011520343.3:c.650C>T, XM_011520343.2:c.650C>T, XM_011520343.1:c.650C>T, NM_001042781.3:c.611C>T, NM_001042781.2:c.611C>T, NM_001042782.3:c.593C>T, NM_001042782.2:c.593C>T, NM_001042780.3:c.593C>T, NM_001042780.2:c.593C>T, XM_006718299.3:c.590C>T, XM_006718299.2:c.590C>T, XM_006718299.1:c.590C>T, NM_001297646.2:c.593C>T, NM_001297646.1:c.593C>T, XM_017018216.2:c.632C>T, XM_017018216.1:c.632C>T, NM_001363561.2:c.626C>T, NM_001363561.1:c.626C>T, XM_017018206.2:c.650C>T, XM_017018206.1:c.650C>T, XM_017018217.2:c.611C>T, XM_017018217.1:c.611C>T, XM_017018205.2:c.611C>T, XM_017018205.1:c.611C>T, XM_017018207.2:c.638C>T, XM_017018207.1:c.638C>T, XM_017018218.2:c.599C>T, XM_017018218.1:c.599C>T, XM_017018209.2:c.614C>T, XM_017018209.1:c.614C>T, XM_024448669.2:c.611C>T, XM_024448669.1:c.611C>T, XM_017018208.2:c.629C>T, XM_017018208.1:c.629C>T, XM_017018219.2:c.560C>T, XM_017018219.1:c.560C>T, XM_017018211.2:c.599C>T, XM_017018211.1:c.599C>T, XM_017018210.2:c.605C>T, XM_017018210.1:c.605C>T, XM_017018212.2:c.596C>T, XM_017018212.1:c.596C>T, XM_024448670.2:c.593C>T, XM_024448670.1:c.593C>T, XM_024448671.2:c.590C>T, XM_024448671.1:c.590C>T, XM_017018213.2:c.581C>T, XM_017018213.1:c.581C>T, XM_017018214.2:c.578C>T, XM_017018214.1:c.578C>T, XM_024448672.2:c.572C>T, XM_024448672.1:c.572C>T, XM_017018215.2:c.572C>T, XM_017018215.1:c.572C>T, NM_001367846.1:c.650C>T, NM_001367848.1:c.614C>T, NM_001367843.1:c.611C>T, NM_001367845.1:c.593C>T, NM_001367847.1:c.626C>T, NM_001367842.1:c.611C>T, NM_001367850.1:c.560C>T, NM_001367844.1:c.593C>T, NM_001367851.1:c.413C>T, NM_001367852.1:c.413C>T, NM_001367849.1:c.605C>T, XP_006718357.1:p.Thr209Ile, NP_006748.1:p.Thr206Ile, XP_006718363.1:p.Thr193Ile, XP_011518645.1:p.Thr217Ile, NP_001036246.1:p.Thr204Ile, NP_001036247.1:p.Thr198Ile, NP_001036245.1:p.Thr198Ile, XP_006718362.1:p.Thr197Ile, NP_001284575.1:p.Thr198Ile, XP_016873705.1:p.Thr211Ile, NP_001350490.1:p.Thr209Ile, XP_016873695.1:p.Thr217Ile, XP_016873706.1:p.Thr204Ile, XP_016873694.1:p.Thr204Ile, XP_016873696.1:p.Thr213Ile, XP_016873707.1:p.Thr200Ile, XP_016873698.1:p.Thr205Ile, XP_024304437.1:p.Thr204Ile, XP_016873697.1:p.Thr210Ile, XP_016873708.1:p.Thr187Ile, XP_016873700.1:p.Thr200Ile, XP_016873699.1:p.Thr202Ile, XP_016873701.1:p.Thr199Ile, XP_024304438.1:p.Thr198Ile, XP_024304439.1:p.Thr197Ile, XP_016873702.1:p.Thr194Ile, XP_016873703.1:p.Thr193Ile, XP_024304440.1:p.Thr191Ile, XP_016873704.1:p.Thr191Ile, NP_001354775.1:p.Thr217Ile, NP_001354777.1:p.Thr205Ile, NP_001354772.1:p.Thr204Ile, NP_001354774.1:p.Thr198Ile, NP_001354776.1:p.Thr209Ile, NP_001354771.1:p.Thr204Ile, NP_001354779.1:p.Thr187Ile, NP_001354773.1:p.Thr198Ile, NP_001354780.1:p.Thr138Ile, NP_001354781.1:p.Thr138Ile, NP_001354778.1:p.Thr202Ile

                                      19.

                                      rs1420516180 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        11:1925267 (GRCh38)
                                        11:1946497 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:1925266:C:T
                                        Gene:
                                        TNNT3 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,intron_variant,missense_variant
                                        HGVS:
                                        NC_000011.10:g.1925267C>T, NC_000011.9:g.1946497C>T, NW_021160004.1:g.94091C>T, XM_006718294.4:c.79C>T, XM_006718294.3:c.79C>T, XM_006718294.2:c.79C>T, XM_006718294.1:c.79C>T, XM_011520343.3:c.79C>T, XM_011520343.2:c.79C>T, XM_011520343.1:c.79C>T, NM_001042781.3:c.79C>T, NM_001042781.2:c.79C>T, XM_017018216.2:c.61C>T, XM_017018216.1:c.61C>T, NM_001363561.2:c.79C>T, NM_001363561.1:c.79C>T, XM_017018206.2:c.79C>T, XM_017018206.1:c.79C>T, XM_017018205.2:c.79C>T, XM_017018205.1:c.79C>T, XM_017018207.2:c.79C>T, XM_017018207.1:c.79C>T, XM_017018209.2:c.79C>T, XM_017018209.1:c.79C>T, XM_024448669.2:c.79C>T, XM_024448669.1:c.79C>T, XM_017018211.2:c.79C>T, XM_017018211.1:c.79C>T, XM_017018212.2:c.61C>T, XM_017018212.1:c.61C>T, XM_024448670.2:c.61C>T, XM_024448670.1:c.61C>T, XM_017018213.2:c.61C>T, XM_017018213.1:c.61C>T, NM_001367846.1:c.79C>T, NM_001367848.1:c.79C>T, NM_001367843.1:c.79C>T, NM_001367845.1:c.61C>T, NM_001367847.1:c.79C>T, NM_001367842.1:c.79C>T, NM_001367849.1:c.61C>T, XP_006718357.1:p.His27Tyr, XP_011518645.1:p.His27Tyr, NP_001036246.1:p.His27Tyr, XP_016873705.1:p.His21Tyr, NP_001350490.1:p.His27Tyr, XP_016873695.1:p.His27Tyr, XP_016873694.1:p.His27Tyr, XP_016873696.1:p.His27Tyr, XP_016873698.1:p.His27Tyr, XP_024304437.1:p.His27Tyr, XP_016873700.1:p.His27Tyr, XP_016873701.1:p.His21Tyr, XP_024304438.1:p.His21Tyr, XP_016873702.1:p.His21Tyr, NP_001354775.1:p.His27Tyr, NP_001354777.1:p.His27Tyr, NP_001354772.1:p.His27Tyr, NP_001354774.1:p.His21Tyr, NP_001354776.1:p.His27Tyr, NP_001354771.1:p.His27Tyr, NP_001354778.1:p.His21Tyr

                                        20.

                                        rs1416726283 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>G [Show Flanks]
                                          Chromosome:
                                          11:1929827 (GRCh38)
                                          11:1951057 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:1929826:A:G
                                          Gene:
                                          TNNT3 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,missense_variant,5_prime_UTR_variant
                                          HGVS:
                                          NC_000011.10:g.1929827A>G, NC_000011.9:g.1951057A>G, NW_021160004.1:g.98649A>G, XM_006718294.4:c.133A>G, XM_006718294.3:c.133A>G, XM_006718294.2:c.133A>G, XM_006718294.1:c.133A>G, NM_006757.4:c.124A>G, NM_006757.3:c.124A>G, XM_006718300.4:c.85A>G, XM_006718300.3:c.85A>G, XM_006718300.2:c.85A>G, XM_006718300.1:c.85A>G, XM_011520343.3:c.157A>G, XM_011520343.2:c.157A>G, XM_011520343.1:c.157A>G, NM_001042781.3:c.118A>G, NM_001042781.2:c.118A>G, NM_001042782.3:c.100A>G, NM_001042782.2:c.100A>G, NM_001042780.3:c.100A>G, NM_001042780.2:c.100A>G, XM_006718299.3:c.97A>G, XM_006718299.2:c.97A>G, XM_006718299.1:c.97A>G, NM_001297646.2:c.100A>G, NM_001297646.1:c.100A>G, XM_017018216.2:c.139A>G, XM_017018216.1:c.139A>G, NM_001363561.2:c.133A>G, NM_001363561.1:c.133A>G, XM_017018206.2:c.157A>G, XM_017018206.1:c.157A>G, XM_017018217.2:c.118A>G, XM_017018217.1:c.118A>G, XM_017018205.2:c.118A>G, XM_017018205.1:c.118A>G, XM_017018207.2:c.145A>G, XM_017018207.1:c.145A>G, XM_017018218.2:c.106A>G, XM_017018218.1:c.106A>G, XM_017018209.2:c.121A>G, XM_017018209.1:c.121A>G, XM_024448669.2:c.118A>G, XM_024448669.1:c.118A>G, XM_017018208.2:c.136A>G, XM_017018208.1:c.136A>G, XM_017018219.2:c.67A>G, XM_017018219.1:c.67A>G, XM_017018211.2:c.106A>G, XM_017018211.1:c.106A>G, XM_017018210.2:c.112A>G, XM_017018210.1:c.112A>G, XM_017018212.2:c.103A>G, XM_017018212.1:c.103A>G, XM_024448670.2:c.100A>G, XM_024448670.1:c.100A>G, XM_024448671.2:c.97A>G, XM_024448671.1:c.97A>G, XM_017018213.2:c.88A>G, XM_017018213.1:c.88A>G, XM_017018214.2:c.85A>G, XM_017018214.1:c.85A>G, XM_024448672.2:c.79A>G, XM_024448672.1:c.79A>G, XM_017018215.2:c.79A>G, XM_017018215.1:c.79A>G, NM_001367846.1:c.157A>G, NM_001367848.1:c.121A>G, NM_001367843.1:c.118A>G, NM_001367845.1:c.100A>G, NM_001367847.1:c.133A>G, NM_001367842.1:c.118A>G, NM_001367850.1:c.67A>G, NM_001367844.1:c.100A>G, NM_001367851.1:c.-81A>G, NM_001367852.1:c.-81A>G, NM_001367849.1:c.112A>G, XP_006718357.1:p.Lys45Glu, NP_006748.1:p.Lys42Glu, XP_006718363.1:p.Lys29Glu, XP_011518645.1:p.Lys53Glu, NP_001036246.1:p.Lys40Glu, NP_001036247.1:p.Lys34Glu, NP_001036245.1:p.Lys34Glu, XP_006718362.1:p.Lys33Glu, NP_001284575.1:p.Lys34Glu, XP_016873705.1:p.Lys47Glu, NP_001350490.1:p.Lys45Glu, XP_016873695.1:p.Lys53Glu, XP_016873706.1:p.Lys40Glu, XP_016873694.1:p.Lys40Glu, XP_016873696.1:p.Lys49Glu, XP_016873707.1:p.Lys36Glu, XP_016873698.1:p.Lys41Glu, XP_024304437.1:p.Lys40Glu, XP_016873697.1:p.Lys46Glu, XP_016873708.1:p.Lys23Glu, XP_016873700.1:p.Lys36Glu, XP_016873699.1:p.Lys38Glu, XP_016873701.1:p.Lys35Glu, XP_024304438.1:p.Lys34Glu, XP_024304439.1:p.Lys33Glu, XP_016873702.1:p.Lys30Glu, XP_016873703.1:p.Lys29Glu, XP_024304440.1:p.Lys27Glu, XP_016873704.1:p.Lys27Glu, NP_001354775.1:p.Lys53Glu, NP_001354777.1:p.Lys41Glu, NP_001354772.1:p.Lys40Glu, NP_001354774.1:p.Lys34Glu, NP_001354776.1:p.Lys45Glu, NP_001354771.1:p.Lys40Glu, NP_001354779.1:p.Lys23Glu, NP_001354773.1:p.Lys34Glu, NP_001354778.1:p.Lys38Glu

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