Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.55153997G>ACA633906540TNNI3c.549+33C>T (n.549+33C>T)
c.582+33C>T (n.582+33C>T)
n.548+33C>T
c.474+33C>T (n.474+33C>T)
n.377+33C>T
 dbSNP gnomAD v2 gnomAD v4
19g.55153997G=CA2343273684TNNI3c.549+33C= (n.549+33C=)
c.582+33C= (n.582+33C=)
n.548+33C=
c.474+33C= (n.474+33C=)
n.377+33C=
19g.55153997G>TCA2587243543TNNI3c.549+33C>A (n.549+33C>A)
c.582+33C>A (n.582+33C>A)
n.548+33C>A
c.474+33C>A (n.474+33C>A)
n.377+33C>A
 gnomAD v4
19g.55153999A>TCA2576892639TNNI3c.549+31T>A (n.549+31T>A)
c.582+31T>A (n.582+31T>A)
n.548+31T>A
c.474+31T>A (n.474+31T>A)
n.377+31T>A
19g.55154000dupCA2587243544TNNI3c.549+30dup (n.549+30dup)
c.582+30dup (n.582+30dup)
n.548+30dup
c.474+30dup (n.474+30dup)
n.377+30dup
 gnomAD v4
19g.55154001C>ACA2587243546TNNI3c.549+29G>T (n.549+29G>T)
c.582+29G>T (n.582+29G>T)
n.548+29G>T
c.474+29G>T (n.474+29G>T)
n.377+29G>T
 gnomAD v4
19g.55154001C=CA2343273685TNNI3c.549+29G= (n.549+29G=)
c.582+29G= (n.582+29G=)
n.548+29G=
c.474+29G= (n.474+29G=)
n.377+29G=
19g.55154001C>GCA051723TNNI3c.549+29G>C (n.549+29G>C)
c.582+29G>C (n.582+29G>C)
n.548+29G>C
c.474+29G>C (n.474+29G>C)
n.377+29G>C
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154002C>TCA2587243547TNNI3c.549+28G>A (n.549+28G>A)
c.582+28G>A (n.582+28G>A)
n.548+28G>A
c.474+28G>A (n.474+28G>A)
n.377+28G>A
 gnomAD v4
19g.55154003T>ACA997261366TNNI3c.549+27A>T (n.549+27A>T)
c.582+27A>T (n.582+27A>T)
n.548+27A>T
c.474+27A>T (n.474+27A>T)
n.377+27A>T
 dbSNP gnomAD v3 gnomAD v4
19g.55154003T>CCA2549564411TNNI3c.549+27A>G (n.549+27A>G)
c.582+27A>G (n.582+27A>G)
n.548+27A>G
c.474+27A>G (n.474+27A>G)
n.377+27A>G
19g.55154003T=CA2343273686TNNI3c.549+27A= (n.549+27A=)
c.582+27A= (n.582+27A=)
n.548+27A=
c.474+27A= (n.474+27A=)
n.377+27A=
19g.55154004C=CA2343273687TNNI3c.549+26G= (n.549+26G=)
c.582+26G= (n.582+26G=)
n.548+26G=
c.474+26G= (n.474+26G=)
n.377+26G=
19g.55154004C>GCA310148262TNNI3c.549+26G>C (n.549+26G>C)
c.582+26G>C (n.582+26G>C)
n.548+26G>C
c.474+26G>C (n.474+26G>C)
n.377+26G>C
 dbSNP
19g.55154004_55154005delinsCTCA2343273688TNNI3c.549+25_549+26delinsAG (n.549+25_549+26delinsAG)
c.582+25_582+26delinsAG (n.582+25_582+26delinsAG)
n.548+25_548+26delinsAG
c.474+25_474+26delinsAG (n.474+25_474+26delinsAG)
n.377+25_377+26delinsAG
19g.55154005T>ACA2587243550TNNI3c.549+25A>T (n.549+25A>T)
c.582+25A>T (n.582+25A>T)
n.548+25A>T
c.474+25A>T (n.474+25A>T)
n.377+25A>T
 gnomAD v4
19g.55154005T>CCA633906542TNNI3c.549+25A>G (n.549+25A>G)
c.582+25A>G (n.582+25A>G)
n.548+25A>G
c.474+25A>G (n.474+25A>G)
n.377+25A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55154005T=CA2343273689TNNI3c.549+25A= (n.549+25A=)
c.582+25A= (n.582+25A=)
n.548+25A=
c.474+25A= (n.474+25A=)
n.377+25A=
19g.55154007delCA633906541TNNI3c.549+25del (n.549+25del)
c.582+25del (n.582+25del)
n.548+25del
c.474+25del (n.474+25del)
n.377+25del
 dbSNP gnomAD v2
19g.55154007_55154008delinsTCCA2343273690TNNI3c.549+22_549+23delinsGA (n.549+22_549+23delinsGA)
c.582+22_582+23delinsGA (n.582+22_582+23delinsGA)
n.548+22_548+23delinsGA
c.474+22_474+23delinsGA (n.474+22_474+23delinsGA)
n.377+22_377+23delinsGA
19g.55154009delCA2343273691TNNI3c.549+22del (n.549+22del)
c.582+22del (n.582+22del)
n.548+22del
c.474+22del (n.474+22del)
n.377+22del
 dbSNP
19g.55154009C>TCA2587243554TNNI3c.549+21G>A (n.549+21G>A)
c.582+21G>A (n.582+21G>A)
n.548+21G>A
c.474+21G>A (n.474+21G>A)
n.377+21G>A
 gnomAD v4
19g.55154010T>CCA051718TNNI3c.549+20A>G (n.549+20A>G)
c.582+20A>G (n.582+20A>G)
n.548+20A>G
c.474+20A>G (n.474+20A>G)
n.377+20A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154010T=CA2343273692TNNI3c.549+20A= (n.549+20A=)
c.582+20A= (n.582+20A=)
n.548+20A=
c.474+20A= (n.474+20A=)
n.377+20A=
19g.55154011G>TCA2587243557TNNI3c.549+19C>A (n.549+19C>A)
c.582+19C>A (n.582+19C>A)
n.548+19C>A
c.474+19C>A (n.474+19C>A)
n.377+19C>A
 gnomAD v4
19g.55154012G>ACA633906543TNNI3c.549+18C>T (n.549+18C>T)
c.582+18C>T (n.582+18C>T)
n.548+18C>T
c.474+18C>T (n.474+18C>T)
n.377+18C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55154012G=CA2343273693TNNI3c.549+18C= (n.549+18C=)
c.582+18C= (n.582+18C=)
n.548+18C=
c.474+18C= (n.474+18C=)
n.377+18C=
19g.55154012G>TCA2587243560TNNI3c.549+18C>A (n.549+18C>A)
c.582+18C>A (n.582+18C>A)
n.548+18C>A
c.474+18C>A (n.474+18C>A)
n.377+18C>A
 gnomAD v4
19g.55154013C=CA2343273694TNNI3c.549+17G= (n.549+17G=)
c.582+17G= (n.582+17G=)
n.548+17G=
c.474+17G= (n.474+17G=)
n.377+17G=
19g.55154013C>TCA633906544TNNI3c.549+17G>A (n.549+17G>A)
c.582+17G>A (n.582+17G>A)
n.548+17G>A
c.474+17G>A (n.474+17G>A)
n.377+17G>A
 dbSNP gnomAD v2 gnomAD v4
19g.55154014C=CA2343273695TNNI3c.549+16G= (n.549+16G=)
c.582+16G= (n.582+16G=)
n.548+16G=
c.474+16G= (n.474+16G=)
n.377+16G=
19g.55154014C>TCA021865TNNI3c.549+16G>A (n.549+16G>A)
c.582+16G>A (n.582+16G>A)
n.548+16G>A
c.474+16G>A (n.474+16G>A)
n.377+16G>A
 dbSNP gnomAD v4
19g.55154016T>CCA2587243563TNNI3c.549+14A>G (n.549+14A>G)
c.582+14A>G (n.582+14A>G)
n.548+14A>G
c.474+14A>G (n.474+14A>G)
n.377+14A>G
 gnomAD v4
19g.55154017A>CCA2587243564TNNI3c.549+13T>G (n.549+13T>G)
c.582+13T>G (n.582+13T>G)
n.548+13T>G
c.474+13T>G (n.474+13T>G)
n.377+13T>G
 gnomAD v4
19g.55154018G>CCA2587243568TNNI3c.549+12C>G (n.549+12C>G)
c.582+12C>G (n.582+12C>G)
n.548+12C>G
c.474+12C>G (n.474+12C>G)
n.377+12C>G
 gnomAD v4
19g.55154018G>TCA2587243566TNNI3c.549+12C>A (n.549+12C>A)
c.582+12C>A (n.582+12C>A)
n.548+12C>A
c.474+12C>A (n.474+12C>A)
n.377+12C>A
 gnomAD v4
19g.55154019C>ACA2587243569TNNI3c.549+11G>T (n.549+11G>T)
c.582+11G>T (n.582+11G>T)
n.548+11G>T
c.474+11G>T (n.474+11G>T)
n.377+11G>T
 gnomAD v4
19g.55154019C>GCA2587243570TNNI3c.549+11G>C (n.549+11G>C)
c.582+11G>C (n.582+11G>C)
n.548+11G>C
c.474+11G>C (n.474+11G>C)
n.377+11G>C
 gnomAD v4
19g.55154021C=CA2343273696TNNI3c.549+9G= (n.549+9G=)
c.582+9G= (n.582+9G=)
n.548+9G=
c.474+9G= (n.474+9G=)
n.377+9G=
19g.55154021C>GCA2343273697TNNI3c.549+9G>C (n.549+9G>C)
c.582+9G>C (n.582+9G>C)
n.548+9G>C
c.474+9G>C (n.474+9G>C)
n.377+9G>C
 dbSNP
19g.55154022A>CCA997261367TNNI3c.549+8T>G (n.549+8T>G)
c.582+8T>G (n.582+8T>G)
n.548+8T>G
c.474+8T>G (n.474+8T>G)
n.377+8T>G
 gnomAD v3 gnomAD v4
19g.55154026_55154029delCA2580097803TNNI3c.549+4_549+7del (n.549+4_549+7del)
c.582+4_582+7del (n.582+4_582+7del)
n.548+4_548+7del
c.474+4_474+7del (n.474+4_474+7del)
n.377+4_377+7del
 ClinVar
19g.55154024A=CA2343273699TNNI3c.549+6T= (n.549+6T=)
c.582+6T= (n.582+6T=)
n.548+6T=
c.474+6T= (n.474+6T=)
n.377+6T=
19g.55154024A>CCA997261368TNNI3c.549+6T>G (n.549+6T>G)
c.582+6T>G (n.582+6T>G)
n.548+6T>G
c.474+6T>G (n.474+6T>G)
n.377+6T>G
 gnomAD v3 gnomAD v4
19g.55154024A>GCA2343273698TNNI3c.549+6T>C (n.549+6T>C)
c.582+6T>C (n.582+6T>C)
n.548+6T>C
c.474+6T>C (n.474+6T>C)
n.377+6T>C
 dbSNP gnomAD v4
19g.55154024A>TCA997261369TNNI3c.549+6T>A (n.549+6T>A)
c.582+6T>A (n.582+6T>A)
n.548+6T>A
c.474+6T>A (n.474+6T>A)
n.377+6T>A
 gnomAD v3 gnomAD v4
19g.55154025C>TCA2587243573TNNI3c.549+5G>A (n.549+5G>A)
c.582+5G>A (n.582+5G>A)
n.548+5G>A
c.474+5G>A (n.474+5G>A)
n.377+5G>A
 ClinVar gnomAD v4
19g.55154026T>ACA891843807TNNI3c.549+4A>T (n.549+4A>T)
c.582+4A>T (n.582+4A>T)
n.548+4A>T
c.474+4A>T (n.474+4A>T)
n.377+4A>T
 ClinVar dbSNP gnomAD v4
19g.55154026T>CCA633906545TNNI3c.549+4A>G (n.549+4A>G)
c.582+4A>G (n.582+4A>G)
n.548+4A>G
c.474+4A>G (n.474+4A>G)
n.377+4A>G
 dbSNP gnomAD v2 gnomAD v4
19g.55154026T=CA2343273700TNNI3c.549+4A= (n.549+4A=)
c.582+4A= (n.582+4A=)
n.548+4A=
c.474+4A= (n.474+4A=)
n.377+4A=
19g.55154027C>ACA051731TNNI3c.549+3G>T (n.549+3G>T)
c.582+3G>T (n.582+3G>T)
n.548+3G>T
c.474+3G>T (n.474+3G>T)
n.377+3G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154027C=CA2343273701TNNI3c.549+3G= (n.549+3G=)
c.582+3G= (n.582+3G=)
n.548+3G=
c.474+3G= (n.474+3G=)
n.377+3G=
19g.55154027C>TCA2343273702TNNI3c.549+3G>A (n.549+3G>A)
c.582+3G>A (n.582+3G>A)
n.548+3G>A
c.474+3G>A (n.474+3G>A)
n.377+3G>A
 dbSNP
19g.55154028delCA2695229156TNNI3c.549+2del (n.549+2del)
c.582+2del (n.582+2del)
n.548+2del
c.474+2del (n.474+2del)
n.377+2del
19g.55154028A=CA2343273703TNNI3c.549+2T= (n.549+2T=)
c.582+2T= (n.582+2T=)
n.548+2T=
c.474+2T= (n.474+2T=)
n.377+2T=
19g.55154028A>CCA407440171TNNI3c.549+2T>G (n.549+2T>G)
c.582+2T>G (n.582+2T>G)
n.548+2T>G
c.474+2T>G (n.474+2T>G)
n.377+2T>G
 dbSNP gnomAD v3 gnomAD v4
19g.55154028A>GCA407440173TNNI3c.549+2T>C (n.549+2T>C)
c.582+2T>C (n.582+2T>C)
n.548+2T>C
c.474+2T>C (n.474+2T>C)
n.377+2T>C
19g.55154028A>TCA310148267TNNI3c.549+2T>A (n.549+2T>A)
c.582+2T>A (n.582+2T>A)
n.548+2T>A
c.474+2T>A (n.474+2T>A)
n.377+2T>A
 dbSNP gnomAD v3 gnomAD v4
19g.55154028_55154043delinsACCTTCTCGGTGTCCTCA2343273704TNNI3c.536_549+2delinsAGGACACCGAGAAGGT
c.569_582+2delinsAGGACACCGAGAAGGT
n.535_548+2delinsAGGACACCGAGAAGGT
c.461_474+2delinsAGGACACCGAGAAGGT
n.364_377+2delinsAGGACACCGAGAAGGT
19g.55154029C>ACA407440177TNNI3c.549+1G>T (n.549+1G>T)
c.582+1G>T (n.582+1G>T)
n.548+1G>T
c.474+1G>T (n.474+1G>T)
n.377+1G>T
19g.55154029C>GCA407440176TNNI3c.549+1G>C (n.549+1G>C)
c.582+1G>C (n.582+1G>C)
n.548+1G>C
c.474+1G>C (n.474+1G>C)
n.377+1G>C
19g.55154029C>TCA407440175TNNI3c.549+1G>A (n.549+1G>A)
c.582+1G>A (n.582+1G>A)
n.548+1G>A
c.474+1G>A (n.474+1G>A)
n.377+1G>A
19g.55154035_55154049delCA2343273705TNNI3c.536_549+1del
c.569_582+1del
n.535_548+1del
c.461_474+1del
n.364_377+1del
 ClinVar dbSNP
19g.55154030C>ACA407440179TNNI3c.549G>T (p.Lys183Asn)
c.582G>T (p.Lys194Asn)
n.548G>T
c.474G>T (p.Lys158Asn)
n.377G>T
 ClinVar dbSNP
19g.55154030C=CA2343273706TNNI3c.549G= (p.Lys183=)
c.582G= (p.Lys194=)
n.548G=
c.474G= (p.Lys158=)
n.377G=
19g.55154030C>GCA407440180TNNI3c.549G>C (p.Lys183Asn)
c.582G>C (p.Lys194Asn)
n.548G>C
c.474G>C (p.Lys158Asn)
n.377G>C
 dbSNP
19g.55154030C>TCA508989365TNNI3c.549G>A (p.Lys183=)
c.582G>A (p.Lys194=)
n.548G>A
c.474G>A (p.Lys158=)
n.377G>A
19g.55154032_55154034delCA2499225605TNNI3c.547_549del (p.Lys183del)
c.580_582del (p.Lys194del)
n.546_548del
c.472_474del (p.Lys158del)
n.375_377del
 ClinVar dbSNP
19g.55154031T>ACA407440182TNNI3c.548A>T (p.Lys183Met)
c.581A>T (p.Lys194Met)
n.547A>T
c.473A>T (p.Lys158Met)
n.376A>T
19g.55154031T>CCA407440183TNNI3c.548A>G (p.Lys183Arg)
c.581A>G (p.Lys194Arg)
n.547A>G
c.473A>G (p.Lys158Arg)
n.376A>G
 ClinVar
19g.55154031T>GCA021859TNNI3c.548A>C (p.Lys183Thr)
c.581A>C (p.Lys194Thr)
n.547A>C
c.473A>C (p.Lys158Thr)
n.376A>C
 ClinVar dbSNP
19g.55154031T=CA2343273707TNNI3c.548A= (p.Lys183=)
c.581A= (p.Lys194=)
n.547A=
c.473A= (p.Lys158=)
n.376A=
19g.55154031_55154032delinsACCA2580097804TNNI3c.547_548delinsGT (p.Lys183Val)
c.580_581delinsGT (p.Lys194Val)
n.546_547delinsGT
c.472_473delinsGT (p.Lys158Val)
n.375_376delinsGT
 ClinVar
19g.55154032T>ACA407440186TNNI3c.547A>T (p.Lys183Ter)
c.580A>T (p.Lys194Ter)
n.546A>T
c.472A>T (p.Lys158Ter)
n.375A>T
19g.55154032T>CCA021854TNNI3c.547A>G (p.Lys183Glu)
c.580A>G (p.Lys194Glu)
n.546A>G
c.472A>G (p.Lys158Glu)
n.375A>G
 ClinVar dbSNP
19g.55154032T>GCA407440188TNNI3c.547A>C (p.Lys183Gln)
c.580A>C (p.Lys194Gln)
n.546A>C
c.472A>C (p.Lys158Gln)
n.375A>C
19g.55154032T=CA2343273708TNNI3c.547A= (p.Lys183=)
c.580A= (p.Lys194=)
n.546A=
c.472A= (p.Lys158=)
n.375A=
19g.55154033C>ACA407440189TNNI3c.546G>T (p.Glu182Asp)
c.579G>T (p.Glu193Asp)
n.545G>T
c.471G>T (p.Glu157Asp)
n.374G>T
19g.55154033C>GCA407440191TNNI3c.546G>C (p.Glu182Asp)
c.579G>C (p.Glu193Asp)
n.545G>C
c.471G>C (p.Glu157Asp)
n.374G>C
19g.55154033C>TCA508989366TNNI3c.546G>A (p.Glu182=)
c.579G>A (p.Glu193=)
n.545G>A
c.471G>A (p.Glu157=)
n.374G>A
 ClinVar dbSNP
19g.55154034T>ACA407440193TNNI3c.545A>T (p.Glu182Val)
c.578A>T (p.Glu193Val)
n.544A>T
c.470A>T (p.Glu157Val)
n.373A>T
19g.55154034T>CCA407440195TNNI3c.545A>G (p.Glu182Gly)
c.578A>G (p.Glu193Gly)
n.544A>G
c.470A>G (p.Glu157Gly)
n.373A>G
19g.55154034T>GCA407440198TNNI3c.545A>C (p.Glu182Ala)
c.578A>C (p.Glu193Ala)
n.544A>C
c.470A>C (p.Glu157Ala)
n.373A>C
19g.55154035C>ACA407440203TNNI3c.544G>T (p.Glu182Ter)
c.577G>T (p.Glu193Ter)
n.543G>T
c.469G>T (p.Glu157Ter)
n.372G>T
 dbSNP gnomAD v2 gnomAD v4
19g.55154035C=CA2343273709TNNI3c.544G= (p.Glu182=)
c.577G= (p.Glu193=)
n.543G=
c.469G= (p.Glu157=)
n.372G=
19g.55154035C>GCA407440200TNNI3c.544G>C (p.Glu182Gln)
c.577G>C (p.Glu193Gln)
n.543G>C
c.469G>C (p.Glu157Gln)
n.372G>C
19g.55154035C>TCA021848TNNI3c.544G>A (p.Glu182Lys)
c.577G>A (p.Glu193Lys)
n.543G>A
c.469G>A (p.Glu157Lys)
n.372G>A
 ClinVar dbSNP gnomAD v4
19g.55154036G>ACA310148279TNNI3c.543C>T (p.Thr181=)
c.576C>T (p.Thr192=)
n.542C>T
c.468C>T (p.Thr156=)
n.371C>T
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.55154036G>CCA508989367TNNI3c.543C>G (p.Thr181=)
c.576C>G (p.Thr192=)
n.542C>G
c.468C>G (p.Thr156=)
n.371C>G
 ClinVar dbSNP gnomAD v4
19g.55154036G=CA2343273710TNNI3c.543C= (p.Thr181=)
c.576C= (p.Thr192=)
n.542C=
c.468C= (p.Thr156=)
n.371C=
19g.55154036G>TCA508989368TNNI3c.543C>A (p.Thr181=)
c.576C>A (p.Thr192=)
n.542C>A
c.468C>A (p.Thr156=)
n.371C>A
 gnomAD v4
19g.55154037delCA2739289551TNNI3c.543del (p.Glu182ArgfsTer17)
c.576del (p.Glu193ArgfsTer17)
n.542del
c.468del (p.Glu157ArgfsTer17)
n.371del
19g.55154037G>ACA407440205TNNI3c.542C>T (p.Thr181Ile)
c.575C>T (p.Thr192Ile)
n.541C>T
c.467C>T (p.Thr156Ile)
n.370C>T
 dbSNP
19g.55154037G>CCA407440210TNNI3c.542C>G (p.Thr181Ser)
c.575C>G (p.Thr192Ser)
n.541C>G
c.467C>G (p.Thr156Ser)
n.370C>G
19g.55154037G>TCA407440211TNNI3c.542C>A (p.Thr181Asn)
c.575C>A (p.Thr192Asn)
n.541C>A
c.467C>A (p.Thr156Asn)
n.370C>A
 gnomAD v4
19g.55154038T>ACA407440213TNNI3c.541A>T (p.Thr181Ser)
c.574A>T (p.Thr192Ser)
n.540A>T
c.466A>T (p.Thr156Ser)
n.369A>T
19g.55154038T>CCA051716TNNI3c.541A>G (p.Thr181Ala)
c.574A>G (p.Thr192Ala)
n.540A>G
c.466A>G (p.Thr156Ala)
n.369A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154038T>GCA407440216TNNI3c.541A>C (p.Thr181Pro)
c.574A>C (p.Thr192Pro)
n.540A>C
c.466A>C (p.Thr156Pro)
n.369A>C
19g.55154038T=CA2343273711TNNI3c.541A= (p.Thr181=)
c.574A= (p.Thr192=)
n.540A=
c.466A= (p.Thr156=)
n.369A=
19g.55154039G>ACA508989369TNNI3c.540C>T (p.Asp180=)
c.573C>T (p.Asp191=)
n.539C>T
c.465C>T (p.Asp155=)
n.368C>T
19g.55154039G>CCA407440217TNNI3c.540C>G (p.Asp180Glu)
c.573C>G (p.Asp191Glu)
n.539C>G
c.465C>G (p.Asp155Glu)
n.368C>G
19g.55154039G>TCA407440219TNNI3c.540C>A (p.Asp180Glu)
c.573C>A (p.Asp191Glu)
n.539C>A
c.465C>A (p.Asp155Glu)
n.368C>A
 gnomAD v4
19g.55154040T>ACA407440221TNNI3c.539A>T (p.Asp180Val)
c.572A>T (p.Asp191Val)
n.538A>T
c.464A>T (p.Asp155Val)
n.367A>T
19g.55154040T>CCA16609776TNNI3c.539A>G (p.Asp180Gly)
c.572A>G (p.Asp191Gly)
n.538A>G
c.464A>G (p.Asp155Gly)
n.367A>G
 ClinVar dbSNP
19g.55154040T>GCA407440223TNNI3c.539A>C (p.Asp180Ala)
c.572A>C (p.Asp191Ala)
n.538A>C
c.464A>C (p.Asp155Ala)
n.367A>C
19g.55154040T=CA2343273713TNNI3c.539A= (p.Asp180=)
c.572A= (p.Asp191=)
n.538A=
c.464A= (p.Asp155=)
n.367A=
19g.55154040_55154041delinsTCCA2343273712TNNI3c.538_539delinsGA (p.Asp180=)
c.571_572delinsGA (p.Asp191=)
n.537_538delinsGA
c.463_464delinsGA (p.Asp155=)
n.366_367delinsGA
19g.55154044_55154046delCA2580614977TNNI3c.537_539del (p.Glu179del)
c.570_572del (p.Glu190del)
n.536_538del
c.462_464del (p.Glu154del)
n.365_367del
 ClinVar
19g.55154041C>ACA407440225TNNI3c.538G>T (p.Asp180Tyr)
c.571G>T (p.Asp191Tyr)
n.537G>T
c.463G>T (p.Asp155Tyr)
n.366G>T
19g.55154041C=CA2343273714TNNI3c.538G= (p.Asp180=)
c.571G= (p.Asp191=)
n.537G=
c.463G= (p.Asp155=)
n.366G=
19g.55154041C>GCA407440227TNNI3c.538G>C (p.Asp180His)
c.571G>C (p.Asp191His)
n.537G>C
c.463G>C (p.Asp155His)
n.366G>C
19g.55154041C>TCA16616429TNNI3c.538G>A (p.Asp180Asn)
c.571G>A (p.Asp191Asn)
n.537G>A
c.463G>A (p.Asp155Asn)
n.366G>A
 ClinVar dbSNP
19g.55154042delCA10577115TNNI3c.538del (p.Asp180ThrfsTer19)
c.571del (p.Asp191ThrfsTer19)
n.537del
c.463del (p.Asp155ThrfsTer19)
n.366del
 ClinVar dbSNP gnomAD v4
19g.55154042C>ACA407440228TNNI3c.537G>T (p.Glu179Asp)
c.570G>T (p.Glu190Asp)
n.536G>T
c.462G>T (p.Glu154Asp)
n.365G>T
19g.55154042C=CA2343273716TNNI3c.537G= (p.Glu179=)
c.570G= (p.Glu190=)
n.536G=
c.462G= (p.Glu154=)
n.365G=
19g.55154042C>GCA407440230TNNI3c.537G>C (p.Glu179Asp)
c.570G>C (p.Glu190Asp)
n.536G>C
c.462G>C (p.Glu154Asp)
n.365G>C
19g.55154042C>TCA021842TNNI3c.537G>A (p.Glu179=)
c.570G>A (p.Glu190=)
n.536G>A
c.462G>A (p.Glu154=)
n.365G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154042_55154043delinsCTCA2343273715TNNI3c.536_537delinsAG (p.Glu179=)
c.569_570delinsAG (p.Glu190=)
n.535_536delinsAG
c.461_462delinsAG (p.Glu154=)
n.364_365delinsAG
19g.55154043delCA883722022TNNI3c.536del (p.Glu179GlyfsTer20)
c.569del (p.Glu190GlyfsTer20)
n.535del
c.461del (p.Glu154GlyfsTer20)
n.364del
 ClinVar dbSNP
19g.55154043T>ACA407440234TNNI3c.536A>T (p.Glu179Val)
c.569A>T (p.Glu190Val)
n.535A>T
c.461A>T (p.Glu154Val)
n.364A>T
19g.55154043T>CCA407440236TNNI3c.536A>G (p.Glu179Gly)
c.569A>G (p.Glu190Gly)
n.535A>G
c.461A>G (p.Glu154Gly)
n.364A>G
 ClinVar dbSNP
19g.55154043T>GCA407440238TNNI3c.536A>C (p.Glu179Ala)
c.569A>C (p.Glu190Ala)
n.535A>C
c.461A>C (p.Glu154Ala)
n.364A>C
19g.55154044C>ACA407440239TNNI3c.535G>T (p.Glu179Ter)
c.568G>T (p.Glu190Ter)
n.534G>T
c.460G>T (p.Glu154Ter)
n.363G>T
19g.55154044C>GCA407440241TNNI3c.535G>C (p.Glu179Gln)
c.568G>C (p.Glu190Gln)
n.534G>C
c.460G>C (p.Glu154Gln)
n.363G>C
 ClinVar dbSNP
19g.55154044C>TCA407440242TNNI3c.535G>A (p.Glu179Lys)
c.568G>A (p.Glu190Lys)
n.534G>A
c.460G>A (p.Glu154Lys)
n.363G>A
19g.55154044_55154047delinsCCTTCA2343273717TNNI3c.532_535delinsAAGG (p.Lys178=)
c.565_568delinsAAGG (p.Lys189=)
n.531_534delinsAAGG
c.457_460delinsAAGG (p.Lys153=)
n.360_363delinsAAGG
19g.55154045C>ACA407440244TNNI3c.534G>T (p.Lys178Asn)
c.567G>T (p.Lys189Asn)
n.533G>T
c.459G>T (p.Lys153Asn)
n.362G>T
 ClinVar
19g.55154045C=CA2343273718TNNI3c.534G= (p.Lys178=)
c.567G= (p.Lys189=)
n.533G=
c.459G= (p.Lys153=)
n.362G=
19g.55154045C>GCA407440246TNNI3c.534G>C (p.Lys178Asn)
c.567G>C (p.Lys189Asn)
n.533G>C
c.459G>C (p.Lys153Asn)
n.362G>C
19g.55154045C>TCA508989370TNNI3c.534G>A (p.Lys178=)
c.567G>A (p.Lys189=)
n.533G>A
c.459G>A (p.Lys153=)
n.362G>A
 dbSNP gnomAD v3 gnomAD v4
19g.55154049_55154051delCA021828TNNI3c.532_534del (p.Lys178del)
c.565_567del (p.Lys189del)
n.531_533del
c.457_459del (p.Lys153del)
n.360_362del
 ClinVar dbSNP
19g.55154046T>ACA407440251TNNI3c.533A>T (p.Lys178Met)
c.566A>T (p.Lys189Met)
n.532A>T
c.458A>T (p.Lys153Met)
n.361A>T
19g.55154046T>CCA407440249TNNI3c.533A>G (p.Lys178Arg)
c.566A>G (p.Lys189Arg)
n.532A>G
c.458A>G (p.Lys153Arg)
n.361A>G
 ClinVar dbSNP
19g.55154046T>GCA407440248TNNI3c.533A>C (p.Lys178Thr)
c.566A>C (p.Lys189Thr)
n.532A>C
c.458A>C (p.Lys153Thr)
n.361A>C
 ClinVar
19g.55154046T=CA2343273719TNNI3c.533A= (p.Lys178=)
c.566A= (p.Lys189=)
n.532A=
c.458A= (p.Lys153=)
n.361A=
19g.55154047T>ACA407440252TNNI3c.532A>T (p.Lys178Ter)
c.565A>T (p.Lys189Ter)
n.531A>T
c.457A>T (p.Lys153Ter)
n.360A>T
19g.55154047T>CCA021835TNNI3c.532A>G (p.Lys178Glu)
c.565A>G (p.Lys189Glu)
n.531A>G
c.457A>G (p.Lys153Glu)
n.360A>G
 ClinVar dbSNP
19g.55154047T>GCA407440254TNNI3c.532A>C (p.Lys178Gln)
c.565A>C (p.Lys189Gln)
n.531A>C
c.457A>C (p.Lys153Gln)
n.360A>C
19g.55154047T=CA2343273720TNNI3c.532A= (p.Lys178=)
c.565A= (p.Lys189=)
n.531A=
c.457A= (p.Lys153=)
n.360A=
19g.55154048C>ACA407440256TNNI3c.531G>T (p.Lys177Asn)
c.564G>T (p.Lys188Asn)
n.530G>T
c.456G>T (p.Lys152Asn)
n.359G>T
 ClinVar
19g.55154048C>GCA407440257TNNI3c.531G>C (p.Lys177Asn)
c.564G>C (p.Lys188Asn)
n.530G>C
c.456G>C (p.Lys152Asn)
n.359G>C
19g.55154048C>TCA508989371TNNI3c.531G>A (p.Lys177=)
c.564G>A (p.Lys188=)
n.530G>A
c.456G>A (p.Lys152=)
n.359G>A
19g.55154049T>ACA407440259TNNI3c.530A>T (p.Lys177Met)
c.563A>T (p.Lys188Met)
n.529A>T
c.455A>T (p.Lys152Met)
n.358A>T
19g.55154049T>CCA407440262TNNI3c.530A>G (p.Lys177Arg)
c.563A>G (p.Lys188Arg)
n.529A>G
c.455A>G (p.Lys152Arg)
n.358A>G
19g.55154049T>GCA407440263TNNI3c.530A>C (p.Lys177Thr)
c.563A>C (p.Lys188Thr)
n.529A>C
c.455A>C (p.Lys152Thr)
n.358A>C
19g.55154049_55154050delCA2695229157TNNI3c.529_530del (p.Lys177GlufsTer?)
c.562_563del (p.Lys188GlufsTer?)
n.528_529del
c.454_455del (p.Lys152GlufsTer?)
n.357_358del
19g.55154050T>ACA407440264TNNI3c.529A>T (p.Lys177Ter)
c.562A>T (p.Lys188Ter)
n.528A>T
c.454A>T (p.Lys152Ter)
n.357A>T
19g.55154050T>CCA407440265TNNI3c.529A>G (p.Lys177Glu)
c.562A>G (p.Lys188Glu)
n.528A>G
c.454A>G (p.Lys152Glu)
n.357A>G
19g.55154050T>GCA407440266TNNI3c.529A>C (p.Lys177Gln)
c.562A>C (p.Lys188Gln)
n.528A>C
c.454A>C (p.Lys152Gln)
n.357A>C
19g.55154051C>ACA508989372TNNI3c.528G>T (p.Val176=)
c.561G>T (p.Val187=)
n.527G>T
c.453G>T (p.Val151=)
n.356G>T
19g.55154051C>GCA508989373TNNI3c.528G>C (p.Val176=)
c.561G>C (p.Val187=)
n.527G>C
c.453G>C (p.Val151=)
n.356G>C
19g.55154051C>TCA508989374TNNI3c.528G>A (p.Val176=)
c.561G>A (p.Val187=)
n.527G>A
c.453G>A (p.Val151=)
n.356G>A
 gnomAD v4
19g.55154052A=CA2343273721TNNI3c.527T= (p.Val176=)
c.560T= (p.Val187=)
n.526T=
c.452T= (p.Val151=)
n.355T=
19g.55154052A>CCA407440267TNNI3c.527T>G (p.Val176Gly)
c.560T>G (p.Val187Gly)
n.526T>G
c.452T>G (p.Val151Gly)
n.355T>G
 dbSNP gnomAD v3 gnomAD v4
19g.55154052A>GCA407440268TNNI3c.527T>C (p.Val176Ala)
c.560T>C (p.Val187Ala)
n.526T>C
c.452T>C (p.Val151Ala)
n.355T>C
19g.55154052A>TCA407440269TNNI3c.527T>A (p.Val176Glu)
c.560T>A (p.Val187Glu)
n.526T>A
c.452T>A (p.Val151Glu)
n.355T>A
19g.55154053C>ACA407440271TNNI3c.526G>T (p.Val176Leu)
c.559G>T (p.Val187Leu)
n.525G>T
c.451G>T (p.Val151Leu)
n.354G>T
19g.55154053C=CA2343273722TNNI3c.526G= (p.Val176=)
c.559G= (p.Val187=)
n.525G=
c.451G= (p.Val151=)
n.354G=
19g.55154053C>GCA407440270TNNI3c.526G>C (p.Val176Leu)
c.559G>C (p.Val187Leu)
n.525G>C
c.451G>C (p.Val151Leu)
n.354G>C
19g.55154053C>TCA021822TNNI3c.526G>A (p.Val176Met)
c.559G>A (p.Val187Met)
n.525G>A
c.451G>A (p.Val151Met)
n.354G>A
 ClinVar dbSNP
19g.55154054C>ACA407440272TNNI3c.525G>T (p.Gln175His)
c.558G>T (p.Gln186His)
n.524G>T
c.450G>T (p.Gln150His)
n.353G>T
19g.55154054C=CA2343273723TNNI3c.525G= (p.Gln175=)
c.558G= (p.Gln186=)
n.524G=
c.450G= (p.Gln150=)
n.353G=
19g.55154054C>GCA021816TNNI3c.525G>C (p.Gln175His)
c.558G>C (p.Gln186His)
n.524G>C
c.450G>C (p.Gln150His)
n.353G>C
 ClinVar dbSNP
19g.55154054C>TCA508989375TNNI3c.525G>A (p.Gln175=)
c.558G>A (p.Gln186=)
n.524G>A
c.450G>A (p.Gln150=)
n.353G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154055T>ACA407440273TNNI3c.524A>T (p.Gln175Leu)
c.557A>T (p.Gln186Leu)
n.523A>T
c.449A>T (p.Gln150Leu)
n.352A>T
19g.55154055T>CCA407440274TNNI3c.524A>G (p.Gln175Arg)
c.557A>G (p.Gln186Arg)
n.523A>G
c.449A>G (p.Gln150Arg)
n.352A>G
 ClinVar
19g.55154055T>GCA407440275TNNI3c.524A>C (p.Gln175Pro)
c.557A>C (p.Gln186Pro)
n.523A>C
c.449A>C (p.Gln150Pro)
n.352A>C
 ClinVar
19g.55154056G>ACA10581187TNNI3c.523C>T (p.Gln175Ter)
c.556C>T (p.Gln186Ter)
n.522C>T
c.448C>T (p.Gln150Ter)
n.351C>T
 ClinVar dbSNP
19g.55154056G>CCA407440276TNNI3c.523C>G (p.Gln175Glu)
c.556C>G (p.Gln186Glu)
n.522C>G
c.448C>G (p.Gln150Glu)
n.351C>G
19g.55154056G=CA2343273724TNNI3c.523C= (p.Gln175=)
c.556C= (p.Gln186=)
n.522C=
c.448C= (p.Gln150=)
n.351C=
19g.55154056G>TCA407440277TNNI3c.523C>A (p.Gln175Lys)
c.556C>A (p.Gln186Lys)
n.522C>A
c.448C>A (p.Gln150Lys)
n.351C>A
 ClinVar dbSNP
19g.55154057C>ACA407440278TNNI3c.522G>T (p.Lys174Asn)
c.555G>T (p.Lys185Asn)
n.521G>T
c.447G>T (p.Lys149Asn)
n.350G>T
 COSMIC
19g.55154057C=CA2343273725TNNI3c.522G= (p.Lys174=)
c.555G= (p.Lys185=)
n.521G=
c.447G= (p.Lys149=)
n.350G=
19g.55154057C>GCA021810TNNI3c.522G>C (p.Lys174Asn)
c.555G>C (p.Lys185Asn)
n.521G>C
c.447G>C (p.Lys149Asn)
n.350G>C
 ClinVar dbSNP
19g.55154057C>TCA508989376TNNI3c.522G>A (p.Lys174=)
c.555G>A (p.Lys185=)
n.521G>A
c.447G>A (p.Lys149=)
n.350G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154058T>ACA407440279TNNI3c.521A>T (p.Lys174Met)
c.554A>T (p.Lys185Met)
n.520A>T
c.446A>T (p.Lys149Met)
n.349A>T
19g.55154058T>CCA407440280TNNI3c.521A>G (p.Lys174Arg)
c.554A>G (p.Lys185Arg)
n.520A>G
c.446A>G (p.Lys149Arg)
n.349A>G
19g.55154058T>GCA021804TNNI3c.521A>C (p.Lys174Thr)
c.554A>C (p.Lys185Thr)
n.520A>C
c.446A>C (p.Lys149Thr)
n.349A>C
 ClinVar dbSNP
19g.55154058T=CA2343273726TNNI3c.521A= (p.Lys174=)
c.554A= (p.Lys185=)
n.520A=
c.446A= (p.Lys149=)
n.349A=
19g.55154059T>ACA407440283TNNI3c.520A>T (p.Lys174Ter)
c.553A>T (p.Lys185Ter)
n.519A>T
c.445A>T (p.Lys149Ter)
n.348A>T
19g.55154059T>CCA407440282TNNI3c.520A>G (p.Lys174Glu)
c.553A>G (p.Lys185Glu)
n.519A>G
c.445A>G (p.Lys149Glu)
n.348A>G
19g.55154059T>GCA407440281TNNI3c.520A>C (p.Lys174Gln)
c.553A>C (p.Lys185Gln)
n.519A>C
c.445A>C (p.Lys149Gln)
n.348A>C
 ClinVar dbSNP
19g.55154059T=CA2343273727TNNI3c.520A= (p.Lys174=)
c.553A= (p.Lys185=)
n.519A=
c.445A= (p.Lys149=)
n.348A=
19g.55154060G>ACA051699TNNI3c.519C>T (p.Leu173=)
c.552C>T (p.Leu184=)
n.518C>T
c.444C>T (p.Leu148=)
n.347C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.55154060G>CCA508989377TNNI3c.519C>G (p.Leu173=)
c.552C>G (p.Leu184=)
n.518C>G
c.444C>G (p.Leu148=)
n.347C>G
19g.55154060G=CA2343273728TNNI3c.519C= (p.Leu173=)
c.552C= (p.Leu184=)
n.518C=
c.444C= (p.Leu148=)
n.347C=
19g.55154060G>TCA508989378TNNI3c.519C>A (p.Leu173=)
c.552C>A (p.Leu184=)
n.518C>A
c.444C>A (p.Leu148=)
n.347C>A
 gnomAD v4
19g.55154061A>CCA407440284TNNI3c.518T>G (p.Leu173Arg)
c.551T>G (p.Leu184Arg)
n.517T>G
c.443T>G (p.Leu148Arg)
n.346T>G
19g.55154061A>GCA407440285TNNI3c.518T>C (p.Leu173Pro)
c.551T>C (p.Leu184Pro)
n.517T>C
c.443T>C (p.Leu148Pro)
n.346T>C
19g.55154061A>TCA407440286TNNI3c.518T>A (p.Leu173His)
c.551T>A (p.Leu184His)
n.517T>A
c.443T>A (p.Leu148His)
n.346T>A
19g.55154062G>ACA407440287TNNI3c.517C>T (p.Leu173Phe)
c.550C>T (p.Leu184Phe)
n.516C>T
c.442C>T (p.Leu148Phe)
n.345C>T
19g.55154062G>CCA407440288TNNI3c.517C>G (p.Leu173Val)
c.550C>G (p.Leu184Val)
n.516C>G
c.442C>G (p.Leu148Val)
n.345C>G
19g.55154062G>TCA407440289TNNI3c.517C>A (p.Leu173Ile)
c.550C>A (p.Leu184Ile)
n.516C>A
c.442C>A (p.Leu148Ile)
n.345C>A
19g.55154063G>ACA051692TNNI3c.516C>T (p.His172=)
c.549C>T (p.His183=)
n.515C>T
c.441C>T (p.His147=)
n.344C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154063G>CCA407440290TNNI3c.516C>G (p.His172Gln)
c.549C>G (p.His183Gln)
n.515C>G
c.441C>G (p.His147Gln)
n.344C>G
19g.55154063G=CA2343273729TNNI3c.516C= (p.His172=)
c.549C= (p.His183=)
n.515C=
c.441C= (p.His147=)
n.344C=
19g.55154063G>TCA407440291TNNI3c.516C>A (p.His172Gln)
c.549C>A (p.His183Gln)
n.515C>A
c.441C>A (p.His147Gln)
n.344C>A
19g.55154064T>ACA407440292TNNI3c.515A>T (p.His172Leu)
c.548A>T (p.His183Leu)
n.514A>T
c.440A>T (p.His147Leu)
n.343A>T
19g.55154064T>CCA407440293TNNI3c.515A>G (p.His172Arg)
c.548A>G (p.His183Arg)
n.514A>G
c.440A>G (p.His147Arg)
n.343A>G
19g.55154064T>GCA407440294TNNI3c.515A>C (p.His172Pro)
c.548A>C (p.His183Pro)
n.514A>C
c.440A>C (p.His147Pro)
n.343A>C
19g.55154064_55154094delinsTGGGCCCGCAGGTCCAGGGACTCCTTAGCCCCA2343273730TNNI3c.485_515delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA (p.Arg162=)
c.518_548delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA (p.Arg173=)
n.484_514delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA
c.410_440delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA (p.Arg137=)
n.313_343delinsGGGCTAAGGAGTCCCTGGACCTGCGGGCCCA
19g.55154065G>ACA407440296TNNI3c.514C>T (p.His172Tyr)
c.547C>T (p.His183Tyr)
n.513C>T
c.439C>T (p.His147Tyr)
n.342C>T
 ClinVar dbSNP
19g.55154065G>CCA021797TNNI3c.514C>G (p.His172Asp)
c.547C>G (p.His183Asp)
n.513C>G
c.439C>G (p.His147Asp)
n.342C>G
 ClinVar dbSNP
19g.55154065G=CA2343273731TNNI3c.514C= (p.His172=)
c.547C= (p.His183=)
n.513C=
c.439C= (p.His147=)
n.342C=
19g.55154065G>TCA407440295TNNI3c.514C>A (p.His172Asn)
c.547C>A (p.His183Asn)
n.513C>A
c.439C>A (p.His147Asn)
n.342C>A
19g.55154071_55154100delCA658658863TNNI3c.485_514del (p.Arg162_Ala171del)
c.518_547del (p.Arg173_Ala182del)
n.484_513del
c.410_439del (p.Arg137_Ala146del)
n.313_342del
 ClinVar dbSNP
19g.55154066G>ACA508989379TNNI3c.513C>T (p.Ala171=)
c.546C>T (p.Ala182=)
n.512C>T
c.438C>T (p.Ala146=)
n.341C>T
 gnomAD v4
19g.55154066G>CCA508989380TNNI3c.513C>G (p.Ala171=)
c.546C>G (p.Ala182=)
n.512C>G
c.438C>G (p.Ala146=)
n.341C>G
19g.55154066G>TCA508989381TNNI3c.513C>A (p.Ala171=)
c.546C>A (p.Ala182=)
n.512C>A
c.438C>A (p.Ala146=)
n.341C>A
19g.55154067G>ACA407440297TNNI3c.512C>T (p.Ala171Val)
c.545C>T (p.Ala182Val)
n.511C>T
c.437C>T (p.Ala146Val)
n.340C>T
 ClinVar dbSNP gnomAD v4
19g.55154067G>CCA407440299TNNI3c.512C>G (p.Ala171Gly)
c.545C>G (p.Ala182Gly)
n.511C>G
c.437C>G (p.Ala146Gly)
n.340C>G
19g.55154067G=CA2343273732TNNI3c.512C= (p.Ala171=)
c.545C= (p.Ala182=)
n.511C=
c.437C= (p.Ala146=)
n.340C=
19g.55154067G>TCA407440298TNNI3c.512C>A (p.Ala171Asp)
c.545C>A (p.Ala182Asp)
n.511C>A
c.437C>A (p.Ala146Asp)
n.340C>A
 gnomAD v4
19g.55154068C>ACA407440300TNNI3c.511G>T (p.Ala171Ser)
c.544G>T (p.Ala182Ser)
n.510G>T
c.436G>T (p.Ala146Ser)
n.339G>T
19g.55154068C=CA2343273733TNNI3c.511G= (p.Ala171=)
c.544G= (p.Ala182=)
n.510G=
c.436G= (p.Ala146=)
n.339G=
19g.55154068C>GCA407440301TNNI3c.511G>C (p.Ala171Pro)
c.544G>C (p.Ala182Pro)
n.510G>C
c.436G>C (p.Ala146Pro)
n.339G>C
19g.55154068C>TCA021791TNNI3c.511G>A (p.Ala171Thr)
c.544G>A (p.Ala182Thr)
n.510G>A
c.436G>A (p.Ala146Thr)
n.339G>A
 ClinVar dbSNP gnomAD v4
19g.55154069C>ACA508989382TNNI3c.510G>T (p.Arg170=)
c.543G>T (p.Arg181=)
n.509G>T
c.435G>T (p.Arg145=)
n.338G>T
19g.55154069C>GCA508989383TNNI3c.510G>C (p.Arg170=)
c.543G>C (p.Arg181=)
n.509G>C
c.435G>C (p.Arg145=)
n.338G>C
19g.55154069C>TCA508989384TNNI3c.510G>A (p.Arg170=)
c.543G>A (p.Arg181=)
n.509G>A
c.435G>A (p.Arg145=)
n.338G>A
19g.55154070C>ACA407440302TNNI3c.509G>T (p.Arg170Leu)
c.542G>T (p.Arg181Leu)
n.508G>T
c.434G>T (p.Arg145Leu)
n.337G>T
19g.55154070C=CA2343273734TNNI3c.509G= (p.Arg170=)
c.542G= (p.Arg181=)
n.508G=
c.434G= (p.Arg145=)
n.337G=
19g.55154070C>GCA407440303TNNI3c.509G>C (p.Arg170Pro)
c.542G>C (p.Arg181Pro)
n.508G>C
c.434G>C (p.Arg145Pro)
n.337G>C
 ClinVar
19g.55154070C>TCA021784TNNI3c.509G>A (p.Arg170Gln)
c.542G>A (p.Arg181Gln)
n.508G>A
c.434G>A (p.Arg145Gln)
n.337G>A
 ClinVar dbSNP gnomAD v4 COSMIC
19g.55154071G>ACA021778TNNI3c.508C>T (p.Arg170Trp)
c.541C>T (p.Arg181Trp)
n.507C>T
c.433C>T (p.Arg145Trp)
n.336C>T
 ClinVar dbSNP gnomAD v4
19g.55154071G>CCA021769TNNI3c.508C>G (p.Arg170Gly)
c.541C>G (p.Arg181Gly)
n.507C>G
c.433C>G (p.Arg145Gly)
n.336C>G
 ClinVar dbSNP
19g.55154071G=CA2343273735TNNI3c.508C= (p.Arg170=)
c.541C= (p.Arg181=)
n.507C=
c.433C= (p.Arg145=)
n.336C=
19g.55154071G>TCA508989385TNNI3c.508C>A (p.Arg170=)
c.541C>A (p.Arg181=)
n.507C>A
c.433C>A (p.Arg145=)
n.336C>A
 ClinVar dbSNP gnomAD v4
19g.55154072C>ACA508989386TNNI3c.507G>T (p.Leu169=)
c.540G>T (p.Leu180=)
n.506G>T
c.432G>T (p.Leu144=)
n.335G>T
19g.55154072C=CA2343273736TNNI3c.507G= (p.Leu169=)
c.540G= (p.Leu180=)
n.506G=
c.432G= (p.Leu144=)
n.335G=
19g.55154072C>GCA508989387TNNI3c.507G>C (p.Leu169=)
c.540G>C (p.Leu180=)
n.506G>C
c.432G>C (p.Leu144=)
n.335G>C
19g.55154072C>TCA508989388TNNI3c.507G>A (p.Leu169=)
c.540G>A (p.Leu180=)
n.506G>A
c.432G>A (p.Leu144=)
n.335G>A
 dbSNP gnomAD v2 gnomAD v4
19g.55154073delCA2695229158TNNI3c.506del (p.Leu169ArgfsTer8)
c.539del (p.Leu180ArgfsTer8)
n.505del
c.431del (p.Leu144ArgfsTer8)
n.334del
19g.55154073A>CCA407440304TNNI3c.506T>G (p.Leu169Arg)
c.539T>G (p.Leu180Arg)
n.505T>G
c.431T>G (p.Leu144Arg)
n.334T>G
19g.55154073A>GCA407440305TNNI3c.506T>C (p.Leu169Pro)
c.539T>C (p.Leu180Pro)
n.505T>C
c.431T>C (p.Leu144Pro)
n.334T>C
 ClinVar dbSNP
19g.55154073A>TCA407440306TNNI3c.506T>A (p.Leu169Gln)
c.539T>A (p.Leu180Gln)
n.505T>A
c.431T>A (p.Leu144Gln)
n.334T>A
19g.55154074G>ACA508989389TNNI3c.505C>T (p.Leu169=)
c.538C>T (p.Leu180=)
n.504C>T
c.430C>T (p.Leu144=)
n.333C>T
19g.55154074G>CCA407440307TNNI3c.505C>G (p.Leu169Val)
c.538C>G (p.Leu180Val)
n.504C>G
c.430C>G (p.Leu144Val)
n.333C>G
19g.55154074G>TCA407440308TNNI3c.505C>A (p.Leu169Met)
c.538C>A (p.Leu180Met)
n.504C>A
c.430C>A (p.Leu144Met)
n.333C>A
19g.55154075G>ACA508989390TNNI3c.504C>T (p.Asp168=)
c.537C>T (p.Asp179=)
n.503C>T
c.429C>T (p.Asp143=)
n.332C>T
 gnomAD v4
19g.55154075G>CCA407440309TNNI3c.504C>G (p.Asp168Glu)
c.537C>G (p.Asp179Glu)
n.503C>G
c.429C>G (p.Asp143Glu)
n.332C>G
19g.55154075G=CA2343273737TNNI3c.504C= (p.Asp168=)
c.537C= (p.Asp179=)
n.503C=
c.429C= (p.Asp143=)
n.332C=
19g.55154075G>TCA407440310TNNI3c.504C>A (p.Asp168Glu)
c.537C>A (p.Asp179Glu)
n.503C>A
c.429C>A (p.Asp143Glu)
n.332C>A
 dbSNP gnomAD v2
19g.55154076T>ACA407440311TNNI3c.503A>T (p.Asp168Val)
c.536A>T (p.Asp179Val)
n.502A>T
c.428A>T (p.Asp143Val)
n.331A>T
19g.55154076T>CCA407440312TNNI3c.503A>G (p.Asp168Gly)
c.536A>G (p.Asp179Gly)
n.502A>G
c.428A>G (p.Asp143Gly)
n.331A>G
19g.55154076T>GCA407440313TNNI3c.503A>C (p.Asp168Ala)
c.536A>C (p.Asp179Ala)
n.502A>C
c.428A>C (p.Asp143Ala)
n.331A>C
19g.55154077C>ACA407440314TNNI3c.502G>T (p.Asp168Tyr)
c.535G>T (p.Asp179Tyr)
n.501G>T
c.427G>T (p.Asp143Tyr)
n.330G>T
 ClinVar
19g.55154077C=CA2343273738TNNI3c.502G= (p.Asp168=)
c.535G= (p.Asp179=)
n.501G=
c.427G= (p.Asp143=)
n.330G=
19g.55154077C>GCA407440315TNNI3c.502G>C (p.Asp168His)
c.535G>C (p.Asp179His)
n.501G>C
c.427G>C (p.Asp143His)
n.330G>C
 ClinVar dbSNP
19g.55154077C>TCA407440316TNNI3c.502G>A (p.Asp168Asn)
c.535G>A (p.Asp179Asn)
n.501G>A
c.427G>A (p.Asp143Asn)
n.330G>A
 ClinVar dbSNP gnomAD v4
19g.55154078delCA2695229159TNNI3c.502del (p.Asp168ThrfsTer9)
c.535del (p.Asp179ThrfsTer9)
n.501del
c.427del (p.Asp143ThrfsTer9)
n.330del
19g.55154078C>ACA508989391TNNI3c.501G>T (p.Leu167=)
c.534G>T (p.Leu178=)
n.500G>T
c.426G>T (p.Leu142=)
n.329G>T
19g.55154078C>GCA508989392TNNI3c.501G>C (p.Leu167=)
c.534G>C (p.Leu178=)
n.500G>C
c.426G>C (p.Leu142=)
n.329G>C
19g.55154078C>TCA508989393TNNI3c.501G>A (p.Leu167=)
c.534G>A (p.Leu178=)
n.500G>A
c.426G>A (p.Leu142=)
n.329G>A
 gnomAD v4
19g.55154079A=CA2343273739TNNI3c.500T= (p.Leu167=)
c.533T= (p.Leu178=)
n.499T=
c.425T= (p.Leu142=)
n.328T=
19g.55154079A>CCA407440317TNNI3c.500T>G (p.Leu167Arg)
c.533T>G (p.Leu178Arg)
n.499T>G
c.425T>G (p.Leu142Arg)
n.328T>G
19g.55154079A>GCA407440318TNNI3c.500T>C (p.Leu167Pro)
c.533T>C (p.Leu178Pro)
n.499T>C
c.425T>C (p.Leu142Pro)
n.328T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154079A>TCA407440319TNNI3c.500T>A (p.Leu167Gln)
c.533T>A (p.Leu178Gln)
n.499T>A
c.425T>A (p.Leu142Gln)
n.328T>A
 gnomAD v4
19g.55154080G>ACA508989394TNNI3c.499C>T (p.Leu167=)
c.532C>T (p.Leu178=)
n.498C>T
c.424C>T (p.Leu142=)
n.327C>T
 dbSNP gnomAD v4
19g.55154080G>CCA407440321TNNI3c.499C>G (p.Leu167Val)
c.532C>G (p.Leu178Val)
n.498C>G
c.424C>G (p.Leu142Val)
n.327C>G
19g.55154080G=CA2343273740TNNI3c.499C= (p.Leu167=)
c.532C= (p.Leu178=)
n.498C=
c.424C= (p.Leu142=)
n.327C=
19g.55154080G>TCA407440322TNNI3c.499C>A (p.Leu167Met)
c.532C>A (p.Leu178Met)
n.498C>A
c.424C>A (p.Leu142Met)
n.327C>A
19g.55154081G>ACA508989397TNNI3c.498C>T (p.Ser166=)
c.531C>T (p.Ser177=)
n.497C>T
c.423C>T (p.Ser141=)
n.326C>T
 COSMIC
19g.55154081G>CCA508989396TNNI3c.498C>G (p.Ser166=)
c.531C>G (p.Ser177=)
n.497C>G
c.423C>G (p.Ser141=)
n.326C>G
19g.55154081G>TCA508989395TNNI3c.498C>A (p.Ser166=)
c.531C>A (p.Ser177=)
n.497C>A
c.423C>A (p.Ser141=)
n.326C>A
19g.55154082G>ACA021763TNNI3c.497C>T (p.Ser166Phe)
c.530C>T (p.Ser177Phe)
n.496C>T
c.422C>T (p.Ser141Phe)
n.325C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154082G>CCA407440326TNNI3c.497C>G (p.Ser166Cys)
c.530C>G (p.Ser177Cys)
n.496C>G
c.422C>G (p.Ser141Cys)
n.325C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55154082G=CA2343273741TNNI3c.497C= (p.Ser166=)
c.530C= (p.Ser177=)
n.496C=
c.422C= (p.Ser141=)
n.325C=
19g.55154082G>TCA407440324TNNI3c.497C>A (p.Ser166Tyr)
c.530C>A (p.Ser177Tyr)
n.496C>A
c.422C>A (p.Ser141Tyr)
n.325C>A
19g.55154083A=CA2343273742TNNI3c.496T= (p.Ser166=)
c.529T= (p.Ser177=)
n.495T=
c.421T= (p.Ser141=)
n.324T=
19g.55154083A>CCA407440327TNNI3c.496T>G (p.Ser166Ala)
c.529T>G (p.Ser177Ala)
n.495T>G
c.421T>G (p.Ser141Ala)
n.324T>G
 dbSNP gnomAD v3 gnomAD v4
19g.55154083A>GCA407440328TNNI3c.496T>C (p.Ser166Pro)
c.529T>C (p.Ser177Pro)
n.495T>C
c.421T>C (p.Ser141Pro)
n.324T>C
 ClinVar dbSNP
19g.55154083A>TCA407440330TNNI3c.496T>A (p.Ser166Thr)
c.529T>A (p.Ser177Thr)
n.495T>A
c.421T>A (p.Ser141Thr)
n.324T>A
19g.55154084C>ACA407440331TNNI3c.495G>T (p.Glu165Asp)
c.528G>T (p.Glu176Asp)
n.494G>T
c.420G>T (p.Glu140Asp)
n.323G>T
19g.55154084C=CA2343273743TNNI3c.495G= (p.Glu165=)
c.528G= (p.Glu176=)
n.494G=
c.420G= (p.Glu140=)
n.323G=
19g.55154084C>GCA407440332TNNI3c.495G>C (p.Glu165Asp)
c.528G>C (p.Glu176Asp)
n.494G>C
c.420G>C (p.Glu140Asp)
n.323G>C
19g.55154084C>TCA508989398TNNI3c.495G>A (p.Glu165=)
c.528G>A (p.Glu176=)
n.494G>A
c.420G>A (p.Glu140=)
n.323G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.55154085T>ACA407440333TNNI3c.494A>T (p.Glu165Val)
c.527A>T (p.Glu176Val)
n.493A>T
c.419A>T (p.Glu140Val)
n.322A>T
19g.55154085T>CCA407440334TNNI3c.494A>G (p.Glu165Gly)
c.527A>G (p.Glu176Gly)
n.493A>G
c.419A>G (p.Glu140Gly)
n.322A>G
19g.55154085T>GCA407440336TNNI3c.494A>C (p.Glu165Ala)
c.527A>C (p.Glu176Ala)
n.493A>C
c.419A>C (p.Glu140Ala)
n.322A>C
19g.55154086C>ACA16608300TNNI3c.493G>T (p.Glu165Ter)
c.526G>T (p.Glu176Ter)
n.492G>T
c.418G>T (p.Glu140Ter)
n.321G>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.55154086C=CA2343273744TNNI3c.493G= (p.Glu165=)
c.526G= (p.Glu176=)
n.492G=
c.418G= (p.Glu140=)
n.321G=
19g.55154086C>GCA407440338TNNI3c.493G>C (p.Glu165Gln)
c.526G>C (p.Glu176Gln)
n.492G>C
c.418G>C (p.Glu140Gln)
n.321G>C
 ClinVar dbSNP
19g.55154086C>TCA407440340TNNI3c.493G>A (p.Glu165Lys)
c.526G>A (p.Glu176Lys)
n.492G>A
c.418G>A (p.Glu140Lys)
n.321G>A
19g.55154087C>ACA407440341TNNI3c.492G>T (p.Lys164Asn)
c.525G>T (p.Lys175Asn)
n.491G>T
c.417G>T (p.Lys139Asn)
n.320G>T
19g.55154087C>GCA407440343TNNI3c.492G>C (p.Lys164Asn)
c.525G>C (p.Lys175Asn)
n.491G>C
c.417G>C (p.Lys139Asn)
n.320G>C
19g.55154087C>TCA508989399TNNI3c.492G>A (p.Lys164=)
c.525G>A (p.Lys175=)
n.491G>A
c.417G>A (p.Lys139=)
n.320G>A
19g.55154088T>ACA407440346TNNI3c.491A>T (p.Lys164Met)
c.524A>T (p.Lys175Met)
n.490A>T
c.416A>T (p.Lys139Met)
n.319A>T
19g.55154088T>CCA407440344TNNI3c.491A>G (p.Lys164Arg)
c.524A>G (p.Lys175Arg)
n.490A>G
c.416A>G (p.Lys139Arg)
n.319A>G
19g.55154088T>GCA310148369TNNI3c.491A>C (p.Lys164Thr)
c.524A>C (p.Lys175Thr)
n.490A>C
c.416A>C (p.Lys139Thr)
n.319A>C
 dbSNP
19g.55154088T=CA2343273745TNNI3c.491A= (p.Lys164=)
c.524A= (p.Lys175=)
n.490A=
c.416A= (p.Lys139=)
n.319A=
19g.55154089T>ACA407440347TNNI3c.490A>T (p.Lys164Ter)
c.523A>T (p.Lys175Ter)
n.489A>T
c.415A>T (p.Lys139Ter)
n.318A>T
19g.55154089T>CCA407440348TNNI3c.490A>G (p.Lys164Glu)
c.523A>G (p.Lys175Glu)
n.489A>G
c.415A>G (p.Lys139Glu)
n.318A>G
 ClinVar
19g.55154089T>GCA407440350TNNI3c.490A>C (p.Lys164Gln)
c.523A>C (p.Lys175Gln)
n.489A>C
c.415A>C (p.Lys139Gln)
n.318A>C
19g.55154090A=CA2343273746TNNI3c.489T= (p.Ala163=)
c.522T= (p.Ala174=)
n.488T=
c.414T= (p.Ala138=)
n.317T=
19g.55154090A>CCA508989400TNNI3c.489T>G (p.Ala163=)
c.522T>G (p.Ala174=)
n.488T>G
c.414T>G (p.Ala138=)
n.317T>G
19g.55154090A>GCA508989401TNNI3c.489T>C (p.Ala163=)
c.522T>C (p.Ala174=)
n.488T>C
c.414T>C (p.Ala138=)
n.317T>C
 dbSNP
19g.55154090A>TCA508989402TNNI3c.489T>A (p.Ala163=)
c.522T>A (p.Ala174=)
n.488T>A
c.414T>A (p.Ala138=)
n.317T>A
19g.55154091G>ACA021757TNNI3c.488C>T (p.Ala163Val)
c.521C>T (p.Ala174Val)
n.487C>T
c.413C>T (p.Ala138Val)
n.316C>T
 ClinVar dbSNP
19g.55154091G>CCA407440352TNNI3c.488C>G (p.Ala163Gly)
c.521C>G (p.Ala174Gly)
n.487C>G
c.413C>G (p.Ala138Gly)
n.316C>G
 ClinVar dbSNP gnomAD v4
19g.55154091G=CA2343273747TNNI3c.488C= (p.Ala163=)
c.521C= (p.Ala174=)
n.487C=
c.413C= (p.Ala138=)
n.316C=
19g.55154091G>TCA407440354TNNI3c.488C>A (p.Ala163Asp)
c.521C>A (p.Ala174Asp)
n.487C>A
c.413C>A (p.Ala138Asp)
n.316C>A
 COSMIC
19g.55154091_55154092delinsGCCA2343273748TNNI3c.487_488delinsGC (p.Ala163=)
c.520_521delinsGC (p.Ala174=)
n.486_487delinsGC
c.412_413delinsGC (p.Ala138=)
n.315_316delinsGC
19g.55154092C>ACA407440355TNNI3c.487G>T (p.Ala163Ser)
c.520G>T (p.Ala174Ser)
n.486G>T
c.412G>T (p.Ala138Ser)
n.315G>T
19g.55154092C>GCA407440357TNNI3c.487G>C (p.Ala163Pro)
c.520G>C (p.Ala174Pro)
n.486G>C
c.412G>C (p.Ala138Pro)
n.315G>C
 ClinVar
19g.55154092C>TCA407440358TNNI3c.487G>A (p.Ala163Thr)
c.520G>A (p.Ala174Thr)
n.486G>A
c.412G>A (p.Ala138Thr)
n.315G>A
 gnomAD v4
19g.55154094dupCA2587243621TNNI3c.487dup (p.Ala163GlyfsTer2)
c.520dup (p.Ala174GlyfsTer2)
n.486dup
c.412dup (p.Ala138GlyfsTer2)
n.315dup
 gnomAD v4
19g.55154094delCA915953049TNNI3c.487del (p.Ala163LeufsTer14)
c.520del (p.Ala174LeufsTer14)
n.486del
c.412del (p.Ala138LeufsTer14)
n.315del
 ClinVar dbSNP
19g.55154093C>ACA508989403TNNI3c.486G>T (p.Arg162=)
c.519G>T (p.Arg173=)
n.485G>T
c.411G>T (p.Arg137=)
n.314G>T
19g.55154093C=CA2343273749TNNI3c.486G= (p.Arg162=)
c.519G= (p.Arg173=)
n.485G=
c.411G= (p.Arg137=)
n.314G=
19g.55154093C>GCA508989404TNNI3c.486G>C (p.Arg162=)
c.519G>C (p.Arg173=)
n.485G>C
c.411G>C (p.Arg137=)
n.314G>C
19g.55154093C>TCA508989405TNNI3c.486G>A (p.Arg162=)
c.519G>A (p.Arg173=)
n.485G>A
c.411G>A (p.Arg137=)
n.314G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.55154094C>ACA407440359TNNI3c.485G>T (p.Arg162Leu)
c.518G>T (p.Arg173Leu)
n.484G>T
c.410G>T (p.Arg137Leu)
n.313G>T
 ClinVar dbSNP
19g.55154094C=CA2343273750TNNI3c.485G= (p.Arg162=)
c.518G= (p.Arg173=)
n.484G=
c.410G= (p.Arg137=)
n.313G=
19g.55154094C>GCA021749TNNI3c.485G>C (p.Arg162Pro)
c.518G>C (p.Arg173Pro)
n.484G>C
c.410G>C (p.Arg137Pro)
n.313G>C
 ClinVar dbSNP
19g.55154094C>TCA021744TNNI3c.485G>A (p.Arg162Gln)
c.518G>A (p.Arg173Gln)
n.484G>A
c.410G>A (p.Arg137Gln)
n.313G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.55154095G>ACA021738TNNI3c.484C>T (p.Arg162Trp)
c.517C>T (p.Arg173Trp)
n.483C>T
c.409C>T (p.Arg137Trp)
n.312C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154095G>CCA407440362TNNI3c.484C>G (p.Arg162Gly)
c.517C>G (p.Arg173Gly)
n.483C>G
c.409C>G (p.Arg137Gly)
n.312C>G
 dbSNP gnomAD v4
19g.55154095G=CA2343273751TNNI3c.484C= (p.Arg162=)
c.517C= (p.Arg173=)
n.483C=
c.409C= (p.Arg137=)
n.312C=
19g.55154095G>TCA508989406TNNI3c.484C>A (p.Arg162=)
c.517C>A (p.Arg173=)
n.483C>A
c.409C>A (p.Arg137=)
n.312C>A
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.55154096G>ACA508989407TNNI3c.483C>T (p.Ala161=)
c.516C>T (p.Ala172=)
n.482C>T
c.408C>T (p.Ala136=)
n.311C>T
19g.55154096G>CCA508989408TNNI3c.483C>G (p.Ala161=)
c.516C>G (p.Ala172=)
n.482C>G
c.408C>G (p.Ala136=)
n.311C>G
19g.55154096G>TCA508989409TNNI3c.483C>A (p.Ala161=)
c.516C>A (p.Ala172=)
n.482C>A
c.408C>A (p.Ala136=)
n.311C>A
19g.55154097G>ACA051664TNNI3c.482C>T (p.Ala161Val)
c.515C>T (p.Ala172Val)
n.481C>T
c.407C>T (p.Ala136Val)
n.310C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.55154097G>CCA407440366TNNI3c.482C>G (p.Ala161Gly)
c.515C>G (p.Ala172Gly)
n.481C>G
c.407C>G (p.Ala136Gly)
n.310C>G
19g.55154097G=CA2343273752TNNI3c.482C= (p.Ala161=)
c.515C= (p.Ala172=)
n.481C=
c.407C= (p.Ala136=)
n.310C=
19g.55154097G>TCA407440365TNNI3c.482C>A (p.Ala161Asp)
c.515C>A (p.Ala172Asp)
n.481C>A
c.407C>A (p.Ala136Asp)
n.310C>A
19g.55154097_55154098delinsGCCA2343273753TNNI3c.481_482delinsGC (p.Ala161=)
c.514_515delinsGC (p.Ala172=)
n.480_481delinsGC
c.406_407delinsGC (p.Ala136=)
n.309_310delinsGC

Number of alleles fetched