Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23415125T>ACA389035435MYH7c.5429A>T (p.Lys1810Met)
14g.23415125T>CCA389035431MYH7c.5429A>G (p.Lys1810Arg)
14g.23415125T>GCA389035433MYH7c.5429A>C (p.Lys1810Thr)
14g.23415126T>ACA389035438MYH7c.5428A>T (p.Lys1810Ter)
14g.23415126T>CCA389035440MYH7c.5428A>G (p.Lys1810Glu)
14g.23415126T>GCA389035442MYH7c.5428A>C (p.Lys1810Gln)
ClinVar dbSNP
14g.23415127C>ACA389035444MYH7c.5427G>T (p.Lys1809Asn)
14g.23415127C=CA2123462058MYH7c.5427G= (p.Lys1809=)
14g.23415127C>GCA389035445MYH7c.5427G>C (p.Lys1809Asn)
14g.23415127C>TCA485766114MYH7c.5427G>A (p.Lys1809=)
dbSNP
14g.23415128T>ACA389035448MYH7c.5426A>T (p.Lys1809Met)
14g.23415128T>CCA389035453MYH7c.5426A>G (p.Lys1809Arg)
14g.23415128T>GCA389035449MYH7c.5426A>C (p.Lys1809Thr)
14g.23415129T>ACA389035456MYH7c.5425A>T (p.Lys1809Ter)
14g.23415129T>CCA389035458MYH7c.5425A>G (p.Lys1809Glu)
14g.23415129T>GCA389035460MYH7c.5425A>C (p.Lys1809Gln)
14g.23415130G>ACA485766124MYH7c.5424C>T (p.Gly1808=)
14g.23415130G>CCA485766128MYH7c.5424C>G (p.Gly1808=)
14g.23415130G>TCA485766131MYH7c.5424C>A (p.Gly1808=)
ClinVar dbSNP
14g.23415131C>ACA389035463MYH7c.5423G>T (p.Gly1808Val)
14g.23415131C=CA2123462063MYH7c.5423G= (p.Gly1808=)
14g.23415131C>GCA257808971MYH7c.5423G>C (p.Gly1808Ala)
dbSNP gnomAD v4
14g.23415131C>TCA389035466MYH7c.5423G>A (p.Gly1808Asp)
ClinVar dbSNP
14g.23415132C>ACA389035469MYH7c.5422G>T (p.Gly1808Cys)
14g.23415132C=CA2123462073MYH7c.5422G= (p.Gly1808=)
14g.23415132C>GCA389035471MYH7c.5422G>C (p.Gly1808Arg)
14g.23415132C>TCA046762MYH7c.5422G>A (p.Gly1808Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415133G>ACA016114MYH7c.5421C>T (p.Gly1807=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415133G>CCA016107MYH7c.5421C>G (p.Gly1807=)
ClinVar dbSNP gnomAD v4
14g.23415133G=CA2123462093MYH7c.5421C= (p.Gly1807=)
14g.23415133G>TCA046739MYH7c.5421C>A (p.Gly1807=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415134C>ACA389035484MYH7c.5420G>T (p.Gly1807Val)
14g.23415134C>GCA389035482MYH7c.5420G>C (p.Gly1807Ala)
14g.23415134C>TCA389035480MYH7c.5420G>A (p.Gly1807Asp)
ClinVar
14g.23415136delCA2580087924MYH7c.5420del (p.Gly1807AlafsTer?)
ClinVar
14g.23415135C>ACA389035488MYH7c.5419G>T (p.Gly1807Cys)
14g.23415135C=CA2123462107MYH7c.5419G= (p.Gly1807=)
14g.23415135C>GCA389035490MYH7c.5419G>C (p.Gly1807Arg)
14g.23415135C>TCA046717MYH7c.5419G>A (p.Gly1807Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415136C>ACA389035493MYH7c.5418G>T (p.Lys1806Asn)
14g.23415136C>GCA389035495MYH7c.5418G>C (p.Lys1806Asn)
14g.23415136C>TCA485766159MYH7c.5418G>A (p.Lys1806=)
14g.23415137T>ACA389035498MYH7c.5417A>T (p.Lys1806Met)
14g.23415137T>CCA389035499MYH7c.5417A>G (p.Lys1806Arg)
14g.23415137T>GCA389035501MYH7c.5417A>C (p.Lys1806Thr)
14g.23415138T>ACA389035505MYH7c.5416A>T (p.Lys1806Ter)
14g.23415138T>CCA389035507MYH7c.5416A>G (p.Lys1806Glu)
ClinVar dbSNP
14g.23415138T>GCA389035508MYH7c.5416A>C (p.Lys1806Gln)
ClinVar dbSNP
14g.23415138T=CA2123462115MYH7c.5416A= (p.Lys1806=)
14g.23415139G>ACA485766165MYH7c.5415C>T (p.Leu1805=)

Number of alleles fetched