Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23414954_23414962dupCA2624231259MYH7c.5559+34_5559+42dup (n.5559+34_5559+42dup)
gnomAD v4
14g.23414956T>CCA2624231261MYH7c.5559+39A>G (n.5559+39A>G)
gnomAD v4
14g.23414957G>ACA613317615MYH7c.5559+38C>T (n.5559+38C>T)
dbSNP gnomAD v2 gnomAD v4
14g.23414957G>CCA2123461232MYH7c.5559+38C>G (n.5559+38C>G)
dbSNP
14g.23414957G=CA2123461230MYH7c.5559+38C= (n.5559+38C=)
14g.23414958G>TCA2624231262MYH7c.5559+37C>A (n.5559+37C>A)
gnomAD v4
14g.23414959T>CCA704282012MYH7c.5559+36A>G (n.5559+36A>G)
dbSNP gnomAD v3 gnomAD v4
14g.23414959T=CA2123461240MYH7c.5559+36A= (n.5559+36A=)
14g.23414960G>ACA2624231263MYH7c.5559+35C>T (n.5559+35C>T)
gnomAD v4
14g.23414960G>TCA2624231264MYH7c.5559+35C>A (n.5559+35C>A)
gnomAD v4
14g.23414961C=CA2123461242MYH7c.5559+34G= (n.5559+34G=)
14g.23414961C>GCA2624231265MYH7c.5559+34G>C (n.5559+34G>C)
gnomAD v4
14g.23414961C>TCA047283MYH7c.5559+34G>A (n.5559+34G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23414962C>ACA2624231266MYH7c.5559+33G>T (n.5559+33G>T)
gnomAD v4
14g.23414962C>TCA2800863581MYH7c.5559+33G>A (n.5559+33G>A)
14g.23414963A=CA2123461246MYH7c.5559+32T= (n.5559+32T=)
14g.23414963A>GCA047274MYH7c.5559+32T>C (n.5559+32T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414964G>ACA047259MYH7c.5559+31C>T (n.5559+31C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414964G=CA2123461253MYH7c.5559+31C= (n.5559+31C=)
14g.23414965G>ACA047251MYH7c.5559+30C>T (n.5559+30C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23414965G=CA2123461256MYH7c.5559+30C= (n.5559+30C=)
14g.23414965G>TCA047237MYH7c.5559+30C>A (n.5559+30C>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414966G>ACA257808662MYH7c.5559+29C>T (n.5559+29C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23414966G=CA2123461263MYH7c.5559+29C= (n.5559+29C=)
14g.23414967C>ACA2624231269MYH7c.5559+28G>T (n.5559+28G>T)
gnomAD v4
14g.23414967C=CA2123461273MYH7c.5559+28G= (n.5559+28G=)
14g.23414967C>TCA047222MYH7c.5559+28G>A (n.5559+28G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414969C>ACA2624231272MYH7c.5559+26G>T (n.5559+26G>T)
gnomAD v4
14g.23414969C=CA2123461296MYH7c.5559+26G= (n.5559+26G=)
14g.23414969C>GCA613317616MYH7c.5559+26G>C (n.5559+26G>C)
dbSNP gnomAD v2 gnomAD v4
14g.23414971G>TCA2624231275MYH7c.5559+24C>A (n.5559+24C>A)
gnomAD v4
14g.23414972C>ACA047212MYH7c.5559+23G>T (n.5559+23G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23414972C=CA2123461299MYH7c.5559+23G= (n.5559+23G=)
14g.23414973C=CA2123461301MYH7c.5559+22G= (n.5559+22G=)
14g.23414973C>GCA613317618MYH7c.5559+22G>C (n.5559+22G>C)
dbSNP gnomAD v2 gnomAD v4
14g.23414974T>CCA2624231283MYH7c.5559+21A>G (n.5559+21A>G)
gnomAD v4
14g.23414975G>ACA2123461306MYH7c.5559+20C>T (n.5559+20C>T)
dbSNP gnomAD v4
14g.23414975G=CA2123461304MYH7c.5559+20C= (n.5559+20C=)
14g.23414975G>TCA2624231290MYH7c.5559+20C>A (n.5559+20C>A)
gnomAD v4
14g.23414976G=CA2123461309MYH7c.5559+19C= (n.5559+19C=)
14g.23414976G>TCA047207MYH7c.5559+19C>A (n.5559+19C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23414978G>TCA2624231292MYH7c.5559+17C>A (n.5559+17C>A)
gnomAD v4
14g.23414979T>ACA613317621MYH7c.5559+16A>T (n.5559+16A>T)
dbSNP gnomAD v2 gnomAD v4
14g.23414979T>CCA2624231293MYH7c.5559+16A>G (n.5559+16A>G)
gnomAD v4
14g.23414979T=CA2123461317MYH7c.5559+16A= (n.5559+16A=)
14g.23414980C>TCA2624231295MYH7c.5559+15G>A (n.5559+15G>A)
gnomAD v4
14g.23414982C>ACA2624231302MYH7c.5559+13G>T (n.5559+13G>T)
gnomAD v4
14g.23414982C=CA2123461322MYH7c.5559+13G= (n.5559+13G=)
14g.23414982C>TCA704282028MYH7c.5559+13G>A (n.5559+13G>A)
ClinVar dbSNP gnomAD v4
14g.23414983C=CA2123461332MYH7c.5559+12G= (n.5559+12G=)
14g.23414983C>TCA047201MYH7c.5559+12G>A (n.5559+12G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414984G>ACA016229MYH7c.5559+11C>T (n.5559+11C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414984G=CA2123461337MYH7c.5559+11C= (n.5559+11C=)
14g.23414984G>TCA2624231315MYH7c.5559+11C>A (n.5559+11C>A)
gnomAD v4
14g.23414985C=CA2123461341MYH7c.5559+10G= (n.5559+10G=)
14g.23414985C>TCA613317623MYH7c.5559+10G>A (n.5559+10G>A)
ClinVar dbSNP gnomAD v2
14g.23414986C>ACA2504413103MYH7c.5559+9G>T (n.5559+9G>T)
14g.23414986C=CA2123461346MYH7c.5559+9G= (n.5559+9G=)
14g.23414986C>TCA016248MYH7c.5559+9G>A (n.5559+9G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23414987C>ACA2624231341MYH7c.5559+8G>T (n.5559+8G>T)
gnomAD v4
14g.23414987C=CA2123461356MYH7c.5559+8G= (n.5559+8G=)
14g.23414987C>TCA016240MYH7c.5559+8G>A (n.5559+8G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414988_23414992delCA2624231336MYH7c.5559+4_5559+8del (n.5559+4_5559+8del)
gnomAD v4
14g.23414988G>ACA047325MYH7c.5559+7C>T (n.5559+7C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414988G>CCA613317625MYH7c.5559+7C>G (n.5559+7C>G)
dbSNP gnomAD v2 gnomAD v4
14g.23414988G=CA2123461365MYH7c.5559+7C= (n.5559+7C=)
14g.23414988G>TCA2624231358MYH7c.5559+7C>A (n.5559+7C>A)
gnomAD v4
14g.23414989T>CCA047320MYH7c.5559+6A>G (n.5559+6A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23414989T=CA2123461374MYH7c.5559+6A= (n.5559+6A=)
14g.23414990C=CA2123461376MYH7c.5559+5G= (n.5559+5G=)
14g.23414990C>TCA047308MYH7c.5559+5G>A (n.5559+5G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414991G>ACA016235MYH7c.5559+4C>T (n.5559+4C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414991G>CCA2624231386MYH7c.5559+4C>G (n.5559+4C>G)
gnomAD v4
14g.23414991G=CA2123461381MYH7c.5559+4C= (n.5559+4C=)
14g.23414991G>TCA2624231388MYH7c.5559+4C>A (n.5559+4C>A)
gnomAD v4
14g.23414992C>ACA2624231392MYH7c.5559+3G>T (n.5559+3G>T)
gnomAD v4
14g.23414992C=CA2123461385MYH7c.5559+3G= (n.5559+3G=)
14g.23414992C>TCA704282046MYH7c.5559+3G>A (n.5559+3G>A)
ClinVar dbSNP gnomAD v4
14g.23414993A>CCA389034987MYH7c.5559+2T>G (n.5559+2T>G)
14g.23414993A>GCA389034988MYH7c.5559+2T>C (n.5559+2T>C)
14g.23414993A>TCA389034989MYH7c.5559+2T>A (n.5559+2T>A)
14g.23414994C>ACA389034990MYH7c.5559+1G>T (n.5559+1G>T)
14g.23414994C>GCA389034991MYH7c.5559+1G>C (n.5559+1G>C)
gnomAD v4
14g.23414994C>TCA389034992MYH7c.5559+1G>A (n.5559+1G>A)
14g.23414995C>ACA389034993MYH7c.5559G>T (p.Gln1853His)
14g.23414995C=CA2123461391MYH7c.5559G= (p.Gln1853=)
14g.23414995C>GCA389034994MYH7c.5559G>C (p.Gln1853His)
14g.23414995C>TCA047353MYH7c.5559G>A (p.Gln1853=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23414996T>ACA389034995MYH7c.5558A>T (p.Gln1853Leu)
dbSNP
14g.23414996T>CCA389034996MYH7c.5558A>G (p.Gln1853Arg)
14g.23414996T>GCA389034997MYH7c.5558A>C (p.Gln1853Pro)
14g.23414997G>ACA389034999MYH7c.5557C>T (p.Gln1853Ter)
14g.23414997G>CCA389035000MYH7c.5557C>G (p.Gln1853Glu)
14g.23414997G>TCA389034998MYH7c.5557C>A (p.Gln1853Lys)
14g.23414998G>ACA485765852MYH7c.5556C>T (p.Tyr1852=)
14g.23414998G>CCA016224MYH7c.5556C>G (p.Tyr1852Ter)
ClinVar dbSNP gnomAD v4
14g.23414998G=CA2123461401MYH7c.5556C= (p.Tyr1852=)
14g.23414998G>TCA389035001MYH7c.5556C>A (p.Tyr1852Ter)
gnomAD v4
14g.23414999T>ACA389035002MYH7c.5555A>T (p.Tyr1852Phe)
14g.23414999T>CCA389035003MYH7c.5555A>G (p.Tyr1852Cys)
gnomAD v4
14g.23414999T>GCA389035004MYH7c.5555A>C (p.Tyr1852Ser)
ClinVar dbSNP
14g.23414999T=CA2123461413MYH7c.5555A= (p.Tyr1852=)
14g.23415000A>CCA389035007MYH7c.5554T>G (p.Tyr1852Asp)
14g.23415000A>GCA389035005MYH7c.5554T>C (p.Tyr1852His)
14g.23415000A>TCA389035006MYH7c.5554T>A (p.Tyr1852Asn)
14g.23415000dupCA2695219049MYH7c.5554dup (p.Tyr1852LeufsTer?)
14g.23415001G>ACA485765853MYH7c.5553C>T (p.Thr1851=)
14g.23415001G>CCA485765854MYH7c.5553C>G (p.Thr1851=)
14g.23415001G>TCA485765855MYH7c.5553C>A (p.Thr1851=)
gnomAD v4 COSMIC
14g.23415002G>ACA389035008MYH7c.5552C>T (p.Thr1851Ile)
ClinVar
14g.23415002G>CCA389035009MYH7c.5552C>G (p.Thr1851Ser)
dbSNP gnomAD v2 gnomAD v4
14g.23415002G=CA2123461427MYH7c.5552C= (p.Thr1851=)
14g.23415002G>TCA389035010MYH7c.5552C>A (p.Thr1851Asn)
gnomAD v4
14g.23415003T>ACA389035011MYH7c.5551A>T (p.Thr1851Ser)
14g.23415003T>CCA389035012MYH7c.5551A>G (p.Thr1851Ala)
14g.23415003T>GCA389035013MYH7c.5551A>C (p.Thr1851Pro)
gnomAD v4
14g.23415004G>ACA047184MYH7c.5550C>T (p.Leu1850=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415004G>CCA485765856MYH7c.5550C>G (p.Leu1850=)
14g.23415004G=CA2123461429MYH7c.5550C= (p.Leu1850=)
14g.23415004G>TCA485765857MYH7c.5550C>A (p.Leu1850=)
gnomAD v4
14g.23415005A=CA2123461452MYH7c.5549T= (p.Leu1850=)
14g.23415005A>CCA389035015MYH7c.5549T>G (p.Leu1850Arg)
14g.23415005A>GCA389035014MYH7c.5549T>C (p.Leu1850Pro)
14g.23415005A>TCA389035016MYH7c.5549T>A (p.Leu1850His)
dbSNP gnomAD v2 gnomAD v4
14g.23415006G>ACA389035017MYH7c.5548C>T (p.Leu1850Phe)
ClinVar dbSNP
14g.23415006G>CCA389035018MYH7c.5548C>G (p.Leu1850Val)
14g.23415006G>TCA389035019MYH7c.5548C>A (p.Leu1850Ile)
gnomAD v4
14g.23415007C>ACA389035020MYH7c.5547G>T (p.Glu1849Asp)
14g.23415007C=CA2123461458MYH7c.5547G= (p.Glu1849=)
14g.23415007C>GCA389035021MYH7c.5547G>C (p.Glu1849Asp)
14g.23415007C>TCA485765858MYH7c.5547G>A (p.Glu1849=)
dbSNP gnomAD v2 gnomAD v4
14g.23415008T>ACA389035022MYH7c.5546A>T (p.Glu1849Val)
14g.23415008T>CCA389035023MYH7c.5546A>G (p.Glu1849Gly)
dbSNP
14g.23415008T>GCA389035024MYH7c.5546A>C (p.Glu1849Ala)
14g.23415008T=CA2123461463MYH7c.5546A= (p.Glu1849=)
14g.23415009C>ACA389035025MYH7c.5545G>T (p.Glu1849Ter)
14g.23415009C>GCA389035026MYH7c.5545G>C (p.Glu1849Gln)
14g.23415009C>TCA389035027MYH7c.5545G>A (p.Glu1849Lys)
14g.23415010C>ACA389035028MYH7c.5544G>T (p.Lys1848Asn)
14g.23415010C=CA2123461471MYH7c.5544G= (p.Lys1848=)
14g.23415010C>GCA389035029MYH7c.5544G>C (p.Lys1848Asn)
14g.23415010C>TCA485765862MYH7c.5544G>A (p.Lys1848=)
dbSNP gnomAD v2 gnomAD v4
14g.23415011T>ACA389035032MYH7c.5543A>T (p.Lys1848Met)
14g.23415011T>CCA389035030MYH7c.5543A>G (p.Lys1848Arg)
dbSNP gnomAD v4
14g.23415011T>GCA389035031MYH7c.5543A>C (p.Lys1848Thr)
14g.23415011T=CA2123461474MYH7c.5543A= (p.Lys1848=)
14g.23415012T>ACA389035033MYH7c.5542A>T (p.Lys1848Ter)
14g.23415012T>CCA389035034MYH7c.5542A>G (p.Lys1848Glu)
14g.23415012T>GCA389035035MYH7c.5542A>C (p.Lys1848Gln)
14g.23415013G>ACA485765864MYH7c.5541C>T (p.Ile1847=)
14g.23415013G>CCA389035036MYH7c.5541C>G (p.Ile1847Met)
ClinVar dbSNP
14g.23415013G=CA2123461480MYH7c.5541C= (p.Ile1847=)
14g.23415013G>TCA047173MYH7c.5541C>A (p.Ile1847=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415014A>CCA389035037MYH7c.5540T>G (p.Ile1847Ser)
14g.23415014A>GCA389035038MYH7c.5540T>C (p.Ile1847Thr)
14g.23415014A>TCA389035039MYH7c.5540T>A (p.Ile1847Asn)
gnomAD v4
14g.23415015T>ACA389035040MYH7c.5539A>T (p.Ile1847Phe)
14g.23415015T>CCA389035041MYH7c.5539A>G (p.Ile1847Val)
gnomAD v4
14g.23415015T>GCA389035042MYH7c.5539A>C (p.Ile1847Leu)
14g.23415016G>ACA485765865MYH7c.5538C>T (p.Arg1846=)
dbSNP
14g.23415016G>CCA485765866MYH7c.5538C>G (p.Arg1846=)
14g.23415016G=CA2123461489MYH7c.5538C= (p.Arg1846=)
14g.23415016G>TCA485765867MYH7c.5538C>A (p.Arg1846=)
14g.23415017C>ACA389035044MYH7c.5537G>T (p.Arg1846Leu)
14g.23415017C=CA2123461494MYH7c.5537G= (p.Arg1846=)
14g.23415017C>GCA389035043MYH7c.5537G>C (p.Arg1846Pro)
gnomAD v4
14g.23415017C>TCA047162MYH7c.5537G>A (p.Arg1846His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415018G>ACA016216MYH7c.5536C>T (p.Arg1846Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415018G>CCA257808736MYH7c.5536C>G (p.Arg1846Gly)
ClinVar dbSNP
14g.23415018G=CA2123461507MYH7c.5536C= (p.Arg1846=)
14g.23415018G>TCA389035045MYH7c.5536C>A (p.Arg1846Ser)
dbSNP gnomAD v3 gnomAD v4
14g.23415019C>ACA485765869MYH7c.5535G>T (p.Arg1845=)
14g.23415019C>GCA485765871MYH7c.5535G>C (p.Arg1845=)
14g.23415019C>TCA485765870MYH7c.5535G>A (p.Arg1845=)
14g.23415020C>ACA389035046MYH7c.5534G>T (p.Arg1845Leu)
gnomAD v4
14g.23415020C=CA2123461518MYH7c.5534G= (p.Arg1845=)
14g.23415020C>GCA389035047MYH7c.5534G>C (p.Arg1845Pro)
14g.23415020C>TCA016210MYH7c.5534G>A (p.Arg1845Gln)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
14g.23415021G>ACA016203MYH7c.5533C>T (p.Arg1845Trp)
ClinVar dbSNP gnomAD v4 COSMIC
14g.23415021G>CCA389035048MYH7c.5533C>G (p.Arg1845Gly)
14g.23415021G=CA2123461537MYH7c.5533C= (p.Arg1845=)
14g.23415021G>TCA047143MYH7c.5533C>A (p.Arg1845=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415022C>ACA389035049MYH7c.5532G>T (p.Glu1844Asp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415022C=CA2123461548MYH7c.5532G= (p.Glu1844=)
14g.23415022C>GCA389035050MYH7c.5532G>C (p.Glu1844Asp)
14g.23415022C>TCA485765872MYH7c.5532G>A (p.Glu1844=)
14g.23415023T>ACA389035051MYH7c.5531A>T (p.Glu1844Val)
14g.23415023T>CCA389035052MYH7c.5531A>G (p.Glu1844Gly)
14g.23415023T>GCA389035053MYH7c.5531A>C (p.Glu1844Ala)
14g.23415024C>ACA389035054MYH7c.5530G>T (p.Glu1844Ter)
14g.23415024C=CA2123461553MYH7c.5530G= (p.Glu1844=)
14g.23415024C>GCA389035055MYH7c.5530G>C (p.Glu1844Gln)
14g.23415024C>TCA016196MYH7c.5530G>A (p.Glu1844Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415025G>ACA047110MYH7c.5529C>T (p.Ser1843=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415025G>CCA389035056MYH7c.5529C>G (p.Ser1843Arg)
dbSNP gnomAD v4
14g.23415025G=CA2123461560MYH7c.5529C= (p.Ser1843=)
14g.23415025G>TCA389035057MYH7c.5529C>A (p.Ser1843Arg)
gnomAD v4
14g.23415026C>ACA389035058MYH7c.5528G>T (p.Ser1843Ile)
14g.23415026C=CA2123461599MYH7c.5528G= (p.Ser1843=)
14g.23415026C>GCA389035059MYH7c.5528G>C (p.Ser1843Thr)
ClinVar
14g.23415026C>TCA389035060MYH7c.5528G>A (p.Ser1843Asn)
ClinVar dbSNP
14g.23415027T>ACA389035061MYH7c.5527A>T (p.Ser1843Cys)
14g.23415027T>CCA016188MYH7c.5527A>G (p.Ser1843Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23415027T>GCA389035062MYH7c.5527A>C (p.Ser1843Arg)
14g.23415027T=CA2123461609MYH7c.5527A= (p.Ser1843=)
14g.23415028C>ACA389035063MYH7c.5526G>T (p.Lys1842Asn)
COSMIC
14g.23415028C>GCA389035064MYH7c.5526G>C (p.Lys1842Asn)
14g.23415028C>TCA485765876MYH7c.5526G>A (p.Lys1842=)
14g.23415029T>ACA389035067MYH7c.5525A>T (p.Lys1842Met)
14g.23415029T>CCA389035065MYH7c.5525A>G (p.Lys1842Arg)
gnomAD v4
14g.23415029T>GCA389035066MYH7c.5525A>C (p.Lys1842Thr)
14g.23415030T>ACA389035068MYH7c.5524A>T (p.Lys1842Ter)
14g.23415030T>CCA389035070MYH7c.5524A>G (p.Lys1842Glu)
ClinVar dbSNP gnomAD v4
14g.23415030T>GCA389035069MYH7c.5524A>C (p.Lys1842Gln)
14g.23415031C>ACA389035071MYH7c.5523G>T (p.Arg1841Ser)
14g.23415031C=CA2123461619MYH7c.5523G= (p.Arg1841=)
14g.23415031C>GCA389035072MYH7c.5523G>C (p.Arg1841Ser)
14g.23415031C>TCA485765877MYH7c.5523G>A (p.Arg1841=)
ClinVar dbSNP gnomAD v4
14g.23415032C>ACA389035073MYH7c.5522G>T (p.Arg1841Met)
14g.23415032C>GCA389035075MYH7c.5522G>C (p.Arg1841Thr)
14g.23415032C>TCA389035074MYH7c.5522G>A (p.Arg1841Lys)
14g.23415033T>ACA389035076MYH7c.5521A>T (p.Arg1841Trp)
14g.23415033T>CCA389035077MYH7c.5521A>G (p.Arg1841Gly)
14g.23415033T>GCA485765879MYH7c.5521A>C (p.Arg1841=)
14g.23415034C>ACA389035078MYH7c.5520G>T (p.Met1840Ile)
14g.23415034C>GCA389035079MYH7c.5520G>C (p.Met1840Ile)
COSMIC
14g.23415034C>TCA389035080MYH7c.5520G>A (p.Met1840Ile)
14g.23415035A=CA2123461626MYH7c.5519T= (p.Met1840=)
14g.23415035A>CCA389035081MYH7c.5519T>G (p.Met1840Arg)
14g.23415035A>GCA047097MYH7c.5519T>C (p.Met1840Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415035A>TCA389035082MYH7c.5519T>A (p.Met1840Lys)
14g.23415036T>ACA389035083MYH7c.5518A>T (p.Met1840Leu)
ClinVar dbSNP
14g.23415036T>CCA389035084MYH7c.5518A>G (p.Met1840Val)
dbSNP gnomAD v2 gnomAD v4
14g.23415036T>GCA389035085MYH7c.5518A>C (p.Met1840Leu)
14g.23415036T=CA2123461634MYH7c.5518A= (p.Met1840=)
14g.23415037G>ACA485765883MYH7c.5517C>T (p.Gly1839=)
14g.23415037G>CCA485765885MYH7c.5517C>G (p.Gly1839=)
gnomAD v4
14g.23415037G>TCA485765887MYH7c.5517C>A (p.Gly1839=)
14g.23415038C>ACA389035088MYH7c.5516G>T (p.Gly1839Val)
14g.23415038C=CA2123461642MYH7c.5516G= (p.Gly1839=)
14g.23415038C>GCA389035087MYH7c.5516G>C (p.Gly1839Ala)
14g.23415038C>TCA389035086MYH7c.5516G>A (p.Gly1839Asp)
ClinVar dbSNP gnomAD v4
14g.23415039C>ACA389035089MYH7c.5515G>T (p.Gly1839Cys)
14g.23415039C>GCA389035090MYH7c.5515G>C (p.Gly1839Arg)
14g.23415039C>TCA389035091MYH7c.5515G>A (p.Gly1839Ser)
COSMIC
14g.23415040C>ACA389035092MYH7c.5514G>T (p.Lys1838Asn)
gnomAD v4
14g.23415040C>GCA389035093MYH7c.5514G>C (p.Lys1838Asn)
14g.23415040C>TCA485765893MYH7c.5514G>A (p.Lys1838=)
ClinVar
14g.23415041T>ACA389035094MYH7c.5513A>T (p.Lys1838Met)
14g.23415041T>CCA389035095MYH7c.5513A>G (p.Lys1838Arg)
14g.23415041T>GCA389035096MYH7c.5513A>C (p.Lys1838Thr)
14g.23415042T>ACA389035097MYH7c.5512A>T (p.Lys1838Ter)
14g.23415042T>CCA389035098MYH7c.5512A>G (p.Lys1838Glu)
14g.23415042T>GCA389035099MYH7c.5512A>C (p.Lys1838Gln)
14g.23415043C>ACA485765896MYH7c.5511G>T (p.Val1837=)
14g.23415043C>GCA485765897MYH7c.5511G>C (p.Val1837=)
ClinVar dbSNP
14g.23415043C>TCA485765899MYH7c.5511G>A (p.Val1837=)
14g.23415044A=CA2123461647MYH7c.5510T= (p.Val1837=)
14g.23415044A>CCA389035102MYH7c.5510T>G (p.Val1837Gly)
14g.23415044A>GCA389035101MYH7c.5510T>C (p.Val1837Ala)
dbSNP gnomAD v4 COSMIC
14g.23415044A>TCA389035100MYH7c.5510T>A (p.Val1837Glu)
14g.23415045C>ACA389035103MYH7c.5509G>T (p.Val1837Leu)
COSMIC
14g.23415045C=CA2123461650MYH7c.5509G= (p.Val1837=)
14g.23415045C>GCA389035104MYH7c.5509G>C (p.Val1837Leu)
dbSNP
14g.23415045C>TCA389035105MYH7c.5509G>A (p.Val1837Met)
dbSNP gnomAD v4
14g.23415046C>ACA485765900MYH7c.5508G>T (p.Ser1836=)
14g.23415046C=CA2123461658MYH7c.5508G= (p.Ser1836=)
14g.23415046C>GCA485765901MYH7c.5508G>C (p.Ser1836=)
14g.23415046C>TCA047085MYH7c.5508G>A (p.Ser1836=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415047G>ACA016175MYH7c.5507C>T (p.Ser1836Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415047G>CCA016167MYH7c.5507C>G (p.Ser1836Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415047G=CA2123461670MYH7c.5507C= (p.Ser1836=)
14g.23415047G>TCA389035106MYH7c.5507C>A (p.Ser1836Ter)
14g.23415048A=CA2123461684MYH7c.5506T= (p.Ser1836=)
14g.23415048A>CCA389035107MYH7c.5506T>G (p.Ser1836Ala)
ClinVar dbSNP gnomAD v4
14g.23415048A>GCA389035109MYH7c.5506T>C (p.Ser1836Pro)
14g.23415048A>TCA389035108MYH7c.5506T>A (p.Ser1836Thr)
14g.23415048_23415050delinsACTCA2123461682MYH7c.5504_5506delinsAGT (p.Glu1835=)
14g.23415049C>ACA389035110MYH7c.5505G>T (p.Glu1835Asp)
14g.23415049C=CA2123461701MYH7c.5505G= (p.Glu1835=)
14g.23415049C>GCA389035111MYH7c.5505G>C (p.Glu1835Asp)
ClinVar dbSNP
14g.23415049C>TCA047052MYH7c.5505G>A (p.Glu1835=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415051_23415052delCA047040MYH7c.5504_5505del (p.Glu1835ValfsTer?)
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
14g.23415050T>ACA389035112MYH7c.5504A>T (p.Glu1835Val)
14g.23415050T>CCA389035114MYH7c.5504A>G (p.Glu1835Gly)
dbSNP gnomAD v2
14g.23415050T>GCA389035113MYH7c.5504A>C (p.Glu1835Ala)
14g.23415050T=CA2123461710MYH7c.5504A= (p.Glu1835=)
14g.23415051C>ACA389035115MYH7c.5503G>T (p.Glu1835Ter)
14g.23415051C=CA2123461718MYH7c.5503G= (p.Glu1835=)
14g.23415051C>GCA047034MYH7c.5503G>C (p.Glu1835Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415051C>TCA016161MYH7c.5503G>A (p.Glu1835Lys)
ClinVar dbSNP
14g.23415051_23415054delCA2624231678MYH7c.5500_5503del (p.Ala1834SerfsTer3)
gnomAD v4
14g.23415052T>ACA485765909MYH7c.5502A>T (p.Ala1834=)
14g.23415052T>CCA485765911MYH7c.5502A>G (p.Ala1834=)
ClinVar dbSNP gnomAD v4
14g.23415052T>GCA485765910MYH7c.5502A>C (p.Ala1834=)
14g.23415052T=CA2123461728MYH7c.5502A= (p.Ala1834=)
14g.23415053G>ACA389035116MYH7c.5501C>T (p.Ala1834Val)
14g.23415053G>CCA389035117MYH7c.5501C>G (p.Ala1834Gly)
14g.23415053G>TCA389035118MYH7c.5501C>A (p.Ala1834Glu)
gnomAD v4
14g.23415054C>ACA047025MYH7c.5500G>T (p.Ala1834Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23415054C=CA2123461745MYH7c.5500G= (p.Ala1834=)
14g.23415054C>GCA389035119MYH7c.5500G>C (p.Ala1834Pro)
14g.23415054C>TCA016152MYH7c.5500G>A (p.Ala1834Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23415055G>ACA016148MYH7c.5499C>T (p.Asn1833=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23415055G>CCA389035121MYH7c.5499C>G (p.Asn1833Lys)
14g.23415055G=CA2123461760MYH7c.5499C= (p.Asn1833=)
14g.23415055G>TCA389035120MYH7c.5499C>A (p.Asn1833Lys)
ClinVar
14g.23415056T>ACA389035122MYH7c.5498A>T (p.Asn1833Ile)
14g.23415056T>CCA046966MYH7c.5498A>G (p.Asn1833Ser)
dbSNP ExAC gnomAD v2
14g.23415056T>GCA389035123MYH7c.5498A>C (p.Asn1833Thr)
14g.23415056T=CA2123461766MYH7c.5498A= (p.Asn1833=)

Number of alleles fetched