Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.50210524_50210531dupCA2586537512MYH14c.159_166dup (p.Val56GlyfsTer?)
c.-2132_-2125dup
c.279_286dup (p.Val96GlyfsTer?)
 gnomAD v4
19g.50210531G>ACA406945982MYH14c.166G>A (p.Val56Met)
c.-2125G>A (n.-2125G>A)
c.286G>A (p.Val96Met)
 gnomAD v4
19g.50210531G>CCA406945980MYH14c.166G>C (p.Val56Leu)
c.-2125G>C (n.-2125G>C)
c.286G>C (p.Val96Leu)
19g.50210531G>TCA406945979MYH14c.166G>T (p.Val56Leu)
c.-2125G>T (n.-2125G>T)
c.286G>T (p.Val96Leu)
 gnomAD v4
19g.50210532T>ACA406945984MYH14c.167T>A (p.Val56Glu)
c.-2124T>A (n.-2124T>A)
c.287T>A (p.Val96Glu)
19g.50210532T>CCA406945985MYH14c.167T>C (p.Val56Ala)
c.-2124T>C (n.-2124T>C)
c.287T>C (p.Val96Ala)
 gnomAD v4
19g.50210532T>GCA406945986MYH14c.167T>G (p.Val56Gly)
c.-2124T>G (n.-2124T>G)
c.287T>G (p.Val96Gly)
19g.50210533G>ACA508302563MYH14c.168G>A (p.Val56=)
c.-2123G>A (n.-2123G>A)
c.288G>A (p.Val96=)
 gnomAD v4
19g.50210533G>CCA508302564MYH14c.168G>C (p.Val56=)
c.-2123G>C (n.-2123G>C)
c.288G>C (p.Val96=)
19g.50210533G>TCA508302565MYH14c.168G>T (p.Val56=)
c.-2123G>T (n.-2123G>T)
c.288G>T (p.Val96=)
 gnomAD v4
19g.50210534T>ACA406945989MYH14c.169T>A (p.Trp57Arg)
c.-2122T>A (n.-2122T>A)
c.289T>A (p.Trp97Arg)
19g.50210534T>CCA406945990MYH14c.169T>C (p.Trp57Arg)
c.-2122T>C (n.-2122T>C)
c.289T>C (p.Trp97Arg)
 ClinVar
19g.50210534T>GCA406945992MYH14c.169T>G (p.Trp57Gly)
c.-2122T>G (n.-2122T>G)
c.289T>G (p.Trp97Gly)
19g.50210535G>ACA406945994MYH14c.170G>A (p.Trp57Ter)
c.-2121G>A (n.-2121G>A)
c.290G>A (p.Trp97Ter)
19g.50210535G>CCA406945996MYH14c.170G>C (p.Trp57Ser)
c.-2121G>C (n.-2121G>C)
c.290G>C (p.Trp97Ser)
19g.50210535G>TCA406945997MYH14c.170G>T (p.Trp57Leu)
c.-2121G>T (n.-2121G>T)
c.290G>T (p.Trp97Leu)
 gnomAD v4
19g.50210537delCA913018746MYH14c.172del (p.Val58CysfsTer?)
c.-2119del (n.-2119del)
c.292del (p.Val98CysfsTer?)
19g.50210536G>ACA406945999MYH14c.171G>A (p.Trp57Ter)
c.-2120G>A (n.-2120G>A)
c.291G>A (p.Trp97Ter)
 gnomAD v4
19g.50210536G>CCA406946001MYH14c.171G>C (p.Trp57Cys)
c.-2120G>C (n.-2120G>C)
c.291G>C (p.Trp97Cys)
19g.50210536G>TCA406946003MYH14c.171G>T (p.Trp57Cys)
c.-2120G>T (n.-2120G>T)
c.291G>T (p.Trp97Cys)
 gnomAD v4
19g.50210537G>ACA406946009MYH14c.172G>A (p.Val58Met)
c.-2119G>A (n.-2119G>A)
c.292G>A (p.Val98Met)
 gnomAD v4
19g.50210537G>CCA406946007MYH14c.172G>C (p.Val58Leu)
c.-2119G>C (n.-2119G>C)
c.292G>C (p.Val98Leu)
 dbSNP gnomAD v2 gnomAD v4
19g.50210537G=CA2340790476MYH14c.172G= (p.Val58=)
c.-2119G= (n.-2119G=)
c.292G= (p.Val98=)
19g.50210537G>TCA406946005MYH14c.172G>T (p.Val58Leu)
c.-2119G>T (n.-2119G>T)
c.292G>T (p.Val98Leu)
 gnomAD v4
19g.50210538T>ACA406946011MYH14c.173T>A (p.Val58Glu)
c.-2118T>A (n.-2118T>A)
c.293T>A (p.Val98Glu)
 gnomAD v4
19g.50210538T>CCA406946013MYH14c.173T>C (p.Val58Ala)
c.-2118T>C (n.-2118T>C)
c.293T>C (p.Val98Ala)
 gnomAD v4
19g.50210538T>GCA406946015MYH14c.173T>G (p.Val58Gly)
c.-2118T>G (n.-2118T>G)
c.293T>G (p.Val98Gly)
19g.50210539G>ACA508302566MYH14c.174G>A (p.Val58=)
c.-2117G>A (n.-2117G>A)
c.294G>A (p.Val98=)
 gnomAD v4
19g.50210539G>CCA508302567MYH14c.174G>C (p.Val58=)
c.-2117G>C (n.-2117G>C)
c.294G>C (p.Val98=)
19g.50210539G>TCA508302568MYH14c.174G>T (p.Val58=)
c.-2117G>T (n.-2117G>T)
c.294G>T (p.Val98=)
 gnomAD v4
19g.50210540C>ACA406946017MYH14c.175C>A (p.Pro59Thr)
c.-2116C>A (n.-2116C>A)
c.295C>A (p.Pro99Thr)
 gnomAD v4
19g.50210540C=CA2340790477MYH14c.175C= (p.Pro59=)
c.-2116C= (n.-2116C=)
c.295C= (p.Pro99=)
19g.50210540C>GCA406946019MYH14c.175C>G (p.Pro59Ala)
c.-2116C>G (n.-2116C>G)
c.295C>G (p.Pro99Ala)
 dbSNP gnomAD v4
19g.50210540C>TCA406946021MYH14c.175C>T (p.Pro59Ser)
c.-2116C>T (n.-2116C>T)
c.295C>T (p.Pro99Ser)
 gnomAD v4
19g.50210541C>ACA406946024MYH14c.176C>A (p.Pro59His)
c.-2115C>A (n.-2115C>A)
c.296C>A (p.Pro99His)
 gnomAD v4
19g.50210541C>GCA406946025MYH14c.176C>G (p.Pro59Arg)
c.-2115C>G (n.-2115C>G)
c.296C>G (p.Pro99Arg)
 COSMIC COSMIC COSMIC
19g.50210541C>TCA406946026MYH14c.176C>T (p.Pro59Leu)
c.-2115C>T (n.-2115C>T)
c.296C>T (p.Pro99Leu)
 gnomAD v4
19g.50210542T>ACA508302569MYH14c.177T>A (p.Pro59=)
c.-2114T>A (n.-2114T>A)
c.297T>A (p.Pro99=)
 gnomAD v4
19g.50210542T>CCA508302570MYH14c.177T>C (p.Pro59=)
c.-2114T>C (n.-2114T>C)
c.297T>C (p.Pro99=)
 gnomAD v4
19g.50210542T>GCA508302571MYH14c.177T>G (p.Pro59=)
c.-2114T>G (n.-2114T>G)
c.297T>G (p.Pro99=)
 gnomAD v4
19g.50210543delCA2586537513MYH14c.178del (p.Ser60ArgfsTer?)
c.-2113del (n.-2113del)
c.298del (p.Ser100ArgfsTer?)
 gnomAD v4
19g.50210543T>ACA406946028MYH14c.178T>A (p.Ser60Thr)
c.-2113T>A (n.-2113T>A)
c.298T>A (p.Ser100Thr)
19g.50210543T>CCA406946030MYH14c.178T>C (p.Ser60Pro)
c.-2113T>C (n.-2113T>C)
c.298T>C (p.Ser100Pro)
 gnomAD v4
19g.50210543T>GCA406946032MYH14c.178T>G (p.Ser60Ala)
c.-2113T>G (n.-2113T>G)
c.298T>G (p.Ser100Ala)
19g.50210544C>ACA406946037MYH14c.179C>A (p.Ser60Ter)
c.-2112C>A (n.-2112C>A)
c.299C>A (p.Ser100Ter)
 gnomAD v4
19g.50210544C>GCA406946035MYH14c.179C>G (p.Ser60Trp)
c.-2112C>G (n.-2112C>G)
c.299C>G (p.Ser100Trp)
 gnomAD v4
19g.50210544C>TCA406946034MYH14c.179C>T (p.Ser60Leu)
c.-2112C>T (n.-2112C>T)
c.299C>T (p.Ser100Leu)
 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210545G>ACA508302574MYH14c.180G>A (p.Ser60=)
c.-2111G>A (n.-2111G>A)
c.300G>A (p.Ser100=)
 dbSNP gnomAD v3 gnomAD v4
19g.50210545G>CCA508302573MYH14c.180G>C (p.Ser60=)
c.-2111G>C (n.-2111G>C)
c.300G>C (p.Ser100=)
19g.50210545G=CA2340790478MYH14c.180G= (p.Ser60=)
c.-2111G= (n.-2111G=)
c.300G= (p.Ser100=)
19g.50210545G>TCA508302572MYH14c.180G>T (p.Ser60=)
c.-2111G>T (n.-2111G>T)
c.300G>T (p.Ser100=)
 gnomAD v4
19g.50210546G>ACA406946039MYH14c.181G>A (p.Glu61Lys)
c.-2110G>A (n.-2110G>A)
c.301G>A (p.Glu101Lys)
 dbSNP gnomAD v4
19g.50210546G>CCA9592204MYH14c.181G>C (p.Glu61Gln)
c.-2110G>C (n.-2110G>C)
c.301G>C (p.Glu101Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210546G=CA2340790479MYH14c.181G= (p.Glu61=)
c.-2110G= (n.-2110G=)
c.301G= (p.Glu101=)
19g.50210546G>TCA406946042MYH14c.181G>T (p.Glu61Ter)
c.-2110G>T (n.-2110G>T)
c.301G>T (p.Glu101Ter)
 gnomAD v4
19g.50210547A>CCA406946044MYH14c.182A>C (p.Glu61Ala)
c.-2109A>C (n.-2109A>C)
c.302A>C (p.Glu101Ala)
19g.50210547A>GCA406946046MYH14c.182A>G (p.Glu61Gly)
c.-2109A>G (n.-2109A>G)
c.302A>G (p.Glu101Gly)
 gnomAD v4
19g.50210547A>TCA406946048MYH14c.182A>T (p.Glu61Val)
c.-2109A>T (n.-2109A>T)
c.302A>T (p.Glu101Val)
19g.50210548G>ACA508302575MYH14c.183G>A (p.Glu61=)
c.-2108G>A (n.-2108G>A)
c.303G>A (p.Glu101=)
 gnomAD v4
19g.50210548G>CCA406946052MYH14c.183G>C (p.Glu61Asp)
c.-2108G>C (n.-2108G>C)
c.303G>C (p.Glu101Asp)
19g.50210548G=CA2340790480MYH14c.183G= (p.Glu61=)
c.-2108G= (n.-2108G=)
c.303G= (p.Glu101=)
19g.50210548G>TCA9592205MYH14c.183G>T (p.Glu61Asp)
c.-2108G>T (n.-2108G>T)
c.303G>T (p.Glu101Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.50210549C>ACA406946054MYH14c.184C>A (p.Leu62Ile)
c.-2107C>A (n.-2107C>A)
c.304C>A (p.Leu102Ile)
 dbSNP gnomAD v4
19g.50210549C=CA2340790481MYH14c.184C= (p.Leu62=)
c.-2107C= (n.-2107C=)
c.304C= (p.Leu102=)
19g.50210549C>GCA406946056MYH14c.184C>G (p.Leu62Val)
c.-2107C>G (n.-2107C>G)
c.304C>G (p.Leu102Val)
19g.50210549C>TCA406946058MYH14c.184C>T (p.Leu62Phe)
c.-2107C>T (n.-2107C>T)
c.304C>T (p.Leu102Phe)
 gnomAD v4
19g.50210550T>ACA406946061MYH14c.185T>A (p.Leu62His)
c.-2106T>A (n.-2106T>A)
c.305T>A (p.Leu102His)
 gnomAD v4
19g.50210550T>CCA406946062MYH14c.185T>C (p.Leu62Pro)
c.-2106T>C (n.-2106T>C)
c.305T>C (p.Leu102Pro)
 gnomAD v4
19g.50210550T>GCA406946064MYH14c.185T>G (p.Leu62Arg)
c.-2106T>G (n.-2106T>G)
c.305T>G (p.Leu102Arg)
 gnomAD v4
19g.50210551T>ACA508302576MYH14c.186T>A (p.Leu62=)
c.-2105T>A (n.-2105T>A)
c.306T>A (p.Leu102=)
19g.50210551T>CCA508302577MYH14c.186T>C (p.Leu62=)
c.-2105T>C (n.-2105T>C)
c.306T>C (p.Leu102=)
19g.50210551T>GCA508302578MYH14c.186T>G (p.Leu62=)
c.-2105T>G (n.-2105T>G)
c.306T>G (p.Leu102=)
19g.50210552C>ACA406946070MYH14c.187C>A (p.His63Asn)
c.-2104C>A (n.-2104C>A)
c.307C>A (p.His103Asn)
 gnomAD v4
19g.50210552C=CA2340790482MYH14c.187C= (p.His63=)
c.-2104C= (n.-2104C=)
c.307C= (p.His103=)
19g.50210552C>GCA406946066MYH14c.187C>G (p.His63Asp)
c.-2104C>G (n.-2104C>G)
c.307C>G (p.His103Asp)
19g.50210552C>TCA406946068MYH14c.187C>T (p.His63Tyr)
c.-2104C>T (n.-2104C>T)
c.307C>T (p.His103Tyr)
 dbSNP gnomAD v4
19g.50210553A>CCA406946072MYH14c.188A>C (p.His63Pro)
c.-2103A>C (n.-2103A>C)
c.308A>C (p.His103Pro)
19g.50210553A>GCA406946074MYH14c.188A>G (p.His63Arg)
c.-2103A>G (n.-2103A>G)
c.308A>G (p.His103Arg)
 gnomAD v4
19g.50210553A>TCA406946076MYH14c.188A>T (p.His63Leu)
c.-2103A>T (n.-2103A>T)
c.308A>T (p.His103Leu)
19g.50210554C>ACA406946078MYH14c.189C>A (p.His63Gln)
c.-2102C>A (n.-2102C>A)
c.309C>A (p.His103Gln)
 gnomAD v4
19g.50210554C=CA2340790483MYH14c.189C= (p.His63=)
c.-2102C= (n.-2102C=)
c.309C= (p.His103=)
19g.50210554C>GCA406946079MYH14c.189C>G (p.His63Gln)
c.-2102C>G (n.-2102C>G)
c.309C>G (p.His103Gln)
19g.50210554C>TCA9592206MYH14c.189C>T (p.His63=)
c.-2102C>T (n.-2102C>T)
c.309C>T (p.His103=)
 dbSNP ExAC gnomAD v4
19g.50210555G>ACA406946081MYH14c.190G>A (p.Gly64Arg)
c.-2101G>A (n.-2101G>A)
c.310G>A (p.Gly104Arg)
 gnomAD v4
19g.50210555G>CCA406946083MYH14c.190G>C (p.Gly64Arg)
c.-2101G>C (n.-2101G>C)
c.310G>C (p.Gly104Arg)
19g.50210555G=CA2340790484MYH14c.190G= (p.Gly64=)
c.-2101G= (n.-2101G=)
c.310G= (p.Gly104=)
19g.50210555G>TCA309565474MYH14c.190G>T (p.Gly64Trp)
c.-2101G>T (n.-2101G>T)
c.310G>T (p.Gly104Trp)
 dbSNP gnomAD v4
19g.50210556G>ACA406946086MYH14c.191G>A (p.Gly64Glu)
c.-2100G>A (n.-2100G>A)
c.311G>A (p.Gly104Glu)
 gnomAD v4
19g.50210556G>CCA406946088MYH14c.191G>C (p.Gly64Ala)
c.-2100G>C (n.-2100G>C)
c.311G>C (p.Gly104Ala)
19g.50210556G=CA2340790485MYH14c.191G= (p.Gly64=)
c.-2100G= (n.-2100G=)
c.311G= (p.Gly104=)
19g.50210556G>TCA309565476MYH14c.191G>T (p.Gly64Val)
c.-2100G>T (n.-2100G>T)
c.311G>T (p.Gly104Val)
 dbSNP gnomAD v2 gnomAD v4
19g.50210557G>ACA309565483MYH14c.192G>A (p.Gly64=)
c.-2099G>A (n.-2099G>A)
c.312G>A (p.Gly104=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210557G>CCA508302579MYH14c.192G>C (p.Gly64=)
c.-2099G>C (n.-2099G>C)
c.312G>C (p.Gly104=)
19g.50210557G=CA2340790486MYH14c.192G= (p.Gly64=)
c.-2099G= (n.-2099G=)
c.312G= (p.Gly104=)
19g.50210557G>TCA133468MYH14c.192G>T (p.Gly64=)
c.-2099G>T (n.-2099G>T)
c.312G>T (p.Gly104=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210558T>ACA406946092MYH14c.193T>A (p.Phe65Ile)
c.-2098T>A (n.-2098T>A)
c.313T>A (p.Phe105Ile)
19g.50210558T>CCA406946096MYH14c.193T>C (p.Phe65Leu)
c.-2098T>C (n.-2098T>C)
c.313T>C (p.Phe105Leu)
19g.50210558T>GCA406946094MYH14c.193T>G (p.Phe65Val)
c.-2098T>G (n.-2098T>G)
c.313T>G (p.Phe105Val)
19g.50210559T>ACA406946098MYH14c.194T>A (p.Phe65Tyr)
c.-2097T>A (n.-2097T>A)
c.314T>A (p.Phe105Tyr)
19g.50210559T>CCA406946099MYH14c.194T>C (p.Phe65Ser)
c.-2097T>C (n.-2097T>C)
c.314T>C (p.Phe105Ser)
19g.50210559T>GCA406946101MYH14c.194T>G (p.Phe65Cys)
c.-2097T>G (n.-2097T>G)
c.314T>G (p.Phe105Cys)
19g.50210560C>ACA406946102MYH14c.195C>A (p.Phe65Leu)
c.-2096C>A (n.-2096C>A)
c.315C>A (p.Phe105Leu)
 gnomAD v4
19g.50210560C=CA2340790487MYH14c.195C= (p.Phe65=)
c.-2096C= (n.-2096C=)
c.315C= (p.Phe105=)
19g.50210560C>GCA406946103MYH14c.195C>G (p.Phe65Leu)
c.-2096C>G (n.-2096C>G)
c.315C>G (p.Phe105Leu)
 COSMIC COSMIC COSMIC
19g.50210560C>TCA9592207MYH14c.195C>T (p.Phe65=)
c.-2096C>T (n.-2096C>T)
c.315C>T (p.Phe105=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210561G>ACA406946107MYH14c.196G>A (p.Glu66Lys)
c.-2095G>A (n.-2095G>A)
c.316G>A (p.Glu106Lys)
 dbSNP gnomAD v2 gnomAD v4
19g.50210561G>CCA406946108MYH14c.196G>C (p.Glu66Gln)
c.-2095G>C (n.-2095G>C)
c.316G>C (p.Glu106Gln)
 gnomAD v4
19g.50210561G=CA2340790488MYH14c.196G= (p.Glu66=)
c.-2095G= (n.-2095G=)
c.316G= (p.Glu106=)
19g.50210561G>TCA406946111MYH14c.196G>T (p.Glu66Ter)
c.-2095G>T (n.-2095G>T)
c.316G>T (p.Glu106Ter)
 gnomAD v4
19g.50210562A=CA2340790489MYH14c.197A= (p.Glu66=)
c.-2094A= (n.-2094A=)
c.317A= (p.Glu106=)
19g.50210562A>CCA406946113MYH14c.197A>C (p.Glu66Ala)
c.-2094A>C (n.-2094A>C)
c.317A>C (p.Glu106Ala)
19g.50210562A>GCA406946115MYH14c.197A>G (p.Glu66Gly)
c.-2094A>G (n.-2094A>G)
c.317A>G (p.Glu106Gly)
 gnomAD v4
19g.50210562A>TCA406946117MYH14c.197A>T (p.Glu66Val)
c.-2094A>T (n.-2094A>T)
c.317A>T (p.Glu106Val)
 gnomAD v4
19g.50210563G>ACA9592208MYH14c.198G>A (p.Glu66=)
c.-2093G>A (n.-2093G>A)
c.318G>A (p.Glu106=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210563G>CCA406946119MYH14c.198G>C (p.Glu66Asp)
c.-2093G>C (n.-2093G>C)
c.318G>C (p.Glu106Asp)
19g.50210563G=CA2340790490MYH14c.198G= (p.Glu66=)
c.-2093G= (n.-2093G=)
c.318G= (p.Glu106=)
19g.50210563G>TCA406946121MYH14c.198G>T (p.Glu66Asp)
c.-2093G>T (n.-2093G>T)
c.318G>T (p.Glu106Asp)
 gnomAD v4
19g.50210570_50210572dupCA633896633MYH14c.205_207dup (p.Ala69_Leu70insAla)
c.-2086_-2084dup (n.-2086_-2084dup)
c.325_327dup (p.Ala109_Leu110insAla)
 dbSNP gnomAD v2 gnomAD v4
19g.50210564G>ACA406946124MYH14c.199G>A (p.Ala67Thr)
c.-2092G>A (n.-2092G>A)
c.319G>A (p.Ala107Thr)
 gnomAD v4
19g.50210564G>CCA406946126MYH14c.199G>C (p.Ala67Pro)
c.-2092G>C (n.-2092G>C)
c.319G>C (p.Ala107Pro)
19g.50210564G>TCA406946128MYH14c.199G>T (p.Ala67Ser)
c.-2092G>T (n.-2092G>T)
c.319G>T (p.Ala107Ser)
 gnomAD v4
19g.50210565_50210566delCA2586537514MYH14c.200_201del (p.Ala67GlyfsTer?)
c.-2091_-2090del (n.-2091_-2090del)
c.320_321del (p.Ala107GlyfsTer?)
 gnomAD v4
19g.50210565C>ACA406946130MYH14c.200C>A (p.Ala67Glu)
c.-2091C>A (n.-2091C>A)
c.320C>A (p.Ala107Glu)
 gnomAD v4
19g.50210565C=CA2340790491MYH14c.200C= (p.Ala67=)
c.-2091C= (n.-2091C=)
c.320C= (p.Ala107=)
19g.50210565C>GCA406946132MYH14c.200C>G (p.Ala67Gly)
c.-2091C>G (n.-2091C>G)
c.320C>G (p.Ala107Gly)
19g.50210565C>TCA406946134MYH14c.200C>T (p.Ala67Val)
c.-2091C>T (n.-2091C>T)
c.320C>T (p.Ala107Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210566G>ACA508302580MYH14c.201G>A (p.Ala67=)
c.-2090G>A (n.-2090G>A)
c.321G>A (p.Ala107=)
 dbSNP gnomAD v4
19g.50210566G>CCA508302581MYH14c.201G>C (p.Ala67=)
c.-2090G>C (n.-2090G>C)
c.321G>C (p.Ala107=)
 gnomAD v4
19g.50210566G=CA2340790492MYH14c.201G= (p.Ala67=)
c.-2090G= (n.-2090G=)
c.321G= (p.Ala107=)
19g.50210566G>TCA508302582MYH14c.201G>T (p.Ala67=)
c.-2090G>T (n.-2090G>T)
c.321G>T (p.Ala107=)
 gnomAD v4
19g.50210567G>ACA406946137MYH14c.202G>A (p.Ala68Thr)
c.-2089G>A (n.-2089G>A)
c.322G>A (p.Ala108Thr)
 COSMIC COSMIC COSMIC
19g.50210567G>CCA406946139MYH14c.202G>C (p.Ala68Pro)
c.-2089G>C (n.-2089G>C)
c.322G>C (p.Ala108Pro)
19g.50210567G=CA2340790493MYH14c.202G= (p.Ala68=)
c.-2089G= (n.-2089G=)
c.322G= (p.Ala108=)
19g.50210567G>TCA406946140MYH14c.202G>T (p.Ala68Ser)
c.-2089G>T (n.-2089G>T)
c.322G>T (p.Ala108Ser)
 dbSNP gnomAD v2 gnomAD v4
19g.50210568C>ACA406946144MYH14c.203C>A (p.Ala68Glu)
c.-2088C>A (n.-2088C>A)
c.323C>A (p.Ala108Glu)
 gnomAD v4
19g.50210568C=CA2340790494MYH14c.203C= (p.Ala68=)
c.-2088C= (n.-2088C=)
c.323C= (p.Ala108=)
19g.50210568C>GCA406946145MYH14c.203C>G (p.Ala68Gly)
c.-2088C>G (n.-2088C>G)
c.323C>G (p.Ala108Gly)
19g.50210568C>TCA406946147MYH14c.203C>T (p.Ala68Val)
c.-2088C>T (n.-2088C>T)
c.323C>T (p.Ala108Val)
 dbSNP gnomAD v4
19g.50210569G>ACA9592209MYH14c.204G>A (p.Ala68=)
c.-2087G>A (n.-2087G>A)
c.324G>A (p.Ala108=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210569G>CCA508302583MYH14c.204G>C (p.Ala68=)
c.-2087G>C (n.-2087G>C)
c.324G>C (p.Ala108=)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC
19g.50210569G=CA2340790495MYH14c.204G= (p.Ala68=)
c.-2087G= (n.-2087G=)
c.324G= (p.Ala108=)
19g.50210569G>TCA508302584MYH14c.204G>T (p.Ala68=)
c.-2087G>T (n.-2087G>T)
c.324G>T (p.Ala108=)
 gnomAD v4
19g.50210570G>ACA406946152MYH14c.205G>A (p.Ala69Thr)
c.-2086G>A (n.-2086G>A)
c.325G>A (p.Ala109Thr)
 gnomAD v4
19g.50210570G>CCA406946150MYH14c.205G>C (p.Ala69Pro)
c.-2086G>C (n.-2086G>C)
c.325G>C (p.Ala109Pro)
19g.50210570G>TCA406946154MYH14c.205G>T (p.Ala69Ser)
c.-2086G>T (n.-2086G>T)
c.325G>T (p.Ala109Ser)
19g.50210571C>ACA406946156MYH14c.206C>A (p.Ala69Glu)
c.-2085C>A (n.-2085C>A)
c.326C>A (p.Ala109Glu)
 ClinVar gnomAD v4
19g.50210571C=CA2340790496MYH14c.206C= (p.Ala69=)
c.-2085C= (n.-2085C=)
c.326C= (p.Ala109=)
19g.50210571C>GCA406946159MYH14c.206C>G (p.Ala69Gly)
c.-2085C>G (n.-2085C>G)
c.326C>G (p.Ala109Gly)
19g.50210571C>TCA406946157MYH14c.206C>T (p.Ala69Val)
c.-2085C>T (n.-2085C>T)
c.326C>T (p.Ala109Val)
 dbSNP gnomAD v2 gnomAD v4
19g.50210572G>ACA508302585MYH14c.207G>A (p.Ala69=)
c.-2084G>A (n.-2084G>A)
c.327G>A (p.Ala109=)
 dbSNP gnomAD v4
19g.50210572G>CCA508302586MYH14c.207G>C (p.Ala69=)
c.-2084G>C (n.-2084G>C)
c.327G>C (p.Ala109=)
19g.50210572G=CA2340790497MYH14c.207G= (p.Ala69=)
c.-2084G= (n.-2084G=)
c.327G= (p.Ala109=)
19g.50210572G>TCA508302587MYH14c.207G>T (p.Ala69=)
c.-2084G>T (n.-2084G>T)
c.327G>T (p.Ala109=)
 gnomAD v4
19g.50210573C>ACA406946162MYH14c.208C>A (p.Leu70Met)
c.-2083C>A (n.-2083C>A)
c.328C>A (p.Leu110Met)
 gnomAD v4
19g.50210573C>GCA406946163MYH14c.208C>G (p.Leu70Val)
c.-2083C>G (n.-2083C>G)
c.328C>G (p.Leu110Val)
19g.50210573C>TCA508302588MYH14c.208C>T (p.Leu70=)
c.-2083C>T (n.-2083C>T)
c.328C>T (p.Leu110=)
 ClinVar dbSNP
19g.50210574T>ACA406946166MYH14c.209T>A (p.Leu70Gln)
c.-2082T>A (n.-2082T>A)
c.329T>A (p.Leu110Gln)
19g.50210574T>CCA406946170MYH14c.209T>C (p.Leu70Pro)
c.-2082T>C (n.-2082T>C)
c.329T>C (p.Leu110Pro)
 gnomAD v4
19g.50210574T>GCA406946168MYH14c.209T>G (p.Leu70Arg)
c.-2082T>G (n.-2082T>G)
c.329T>G (p.Leu110Arg)
19g.50210575G>ACA508302589MYH14c.210G>A (p.Leu70=)
c.-2081G>A (n.-2081G>A)
c.330G>A (p.Leu110=)
 gnomAD v4
19g.50210575G>CCA508302590MYH14c.210G>C (p.Leu70=)
c.-2081G>C (n.-2081G>C)
c.330G>C (p.Leu110=)
19g.50210575G>TCA508302591MYH14c.210G>T (p.Leu70=)
c.-2081G>T (n.-2081G>T)
c.330G>T (p.Leu110=)
 gnomAD v4
19g.50210576C>ACA508302592MYH14c.211C>A (p.Arg71=)
c.-2080C>A (n.-2080C>A)
c.331C>A (p.Arg111=)
 gnomAD v4
19g.50210576C=CA2340790498MYH14c.211C= (p.Arg71=)
c.-2080C= (n.-2080C=)
c.331C= (p.Arg111=)
19g.50210576C>GCA406946171MYH14c.211C>G (p.Arg71Gly)
c.-2080C>G (n.-2080C>G)
c.331C>G (p.Arg111Gly)
 gnomAD v4
19g.50210576C>TCA9592210MYH14c.211C>T (p.Arg71Trp)
c.-2080C>T (n.-2080C>T)
c.331C>T (p.Arg111Trp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210577G>ACA309565510MYH14c.212G>A (p.Arg71Gln)
c.-2079G>A (n.-2079G>A)
c.332G>A (p.Arg111Gln)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210577G>CCA406946175MYH14c.212G>C (p.Arg71Pro)
c.-2079G>C (n.-2079G>C)
c.332G>C (p.Arg111Pro)
19g.50210577G=CA2340790499MYH14c.212G= (p.Arg71=)
c.-2079G= (n.-2079G=)
c.332G= (p.Arg111=)
19g.50210577G>TCA406946177MYH14c.212G>T (p.Arg71Leu)
c.-2079G>T (n.-2079G>T)
c.332G>T (p.Arg111Leu)
 gnomAD v4
19g.50210578G>ACA508302593MYH14c.213G>A (p.Arg71=)
c.-2078G>A (n.-2078G>A)
c.333G>A (p.Arg111=)
 gnomAD v4
19g.50210578G>CCA508302595MYH14c.213G>C (p.Arg71=)
c.-2078G>C (n.-2078G>C)
c.333G>C (p.Arg111=)
19g.50210578G>TCA508302594MYH14c.213G>T (p.Arg71=)
c.-2078G>T (n.-2078G>T)
c.333G>T (p.Arg111=)
 gnomAD v4
19g.50210579G>ACA406946179MYH14c.214G>A (p.Asp72Asn)
c.-2077G>A (n.-2077G>A)
c.334G>A (p.Asp112Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.50210579G>CCA406946181MYH14c.214G>C (p.Asp72His)
c.-2077G>C (n.-2077G>C)
c.334G>C (p.Asp112His)
 dbSNP gnomAD v4
19g.50210579G=CA2340790500MYH14c.214G= (p.Asp72=)
c.-2077G= (n.-2077G=)
c.334G= (p.Asp112=)
19g.50210579G>TCA406946183MYH14c.214G>T (p.Asp72Tyr)
c.-2077G>T (n.-2077G>T)
c.334G>T (p.Asp112Tyr)
19g.50210580A>CCA406946185MYH14c.215A>C (p.Asp72Ala)
c.-2076A>C (n.-2076A>C)
c.335A>C (p.Asp112Ala)
19g.50210580A>GCA406946187MYH14c.215A>G (p.Asp72Gly)
c.-2076A>G (n.-2076A>G)
c.335A>G (p.Asp112Gly)
19g.50210580A>TCA406946189MYH14c.215A>T (p.Asp72Val)
c.-2076A>T (n.-2076A>T)
c.335A>T (p.Asp112Val)
19g.50210581C>ACA406946193MYH14c.216C>A (p.Asp72Glu)
c.-2075C>A (n.-2075C>A)
c.336C>A (p.Asp112Glu)
 gnomAD v4
19g.50210581C=CA2340790501MYH14c.216C= (p.Asp72=)
c.-2075C= (n.-2075C=)
c.336C= (p.Asp112=)
19g.50210581C>GCA406946191MYH14c.216C>G (p.Asp72Glu)
c.-2075C>G (n.-2075C>G)
c.336C>G (p.Asp112Glu)
19g.50210581C>TCA309565512MYH14c.216C>T (p.Asp72=)
c.-2075C>T (n.-2075C>T)
c.336C>T (p.Asp112=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210582G>ACA406946195MYH14c.217G>A (p.Glu73Lys)
c.-2074G>A (n.-2074G>A)
c.337G>A (p.Glu113Lys)
 dbSNP gnomAD v4
19g.50210582G>CCA406946197MYH14c.217G>C (p.Glu73Gln)
c.-2074G>C (n.-2074G>C)
c.337G>C (p.Glu113Gln)
19g.50210582G=CA2340790502MYH14c.217G= (p.Glu73=)
c.-2074G= (n.-2074G=)
c.337G= (p.Glu113=)
19g.50210582G>TCA406946199MYH14c.217G>T (p.Glu73Ter)
c.-2074G>T (n.-2074G>T)
c.337G>T (p.Glu113Ter)
 gnomAD v4
19g.50210583A>CCA406946201MYH14c.218A>C (p.Glu73Ala)
c.-2073A>C (n.-2073A>C)
c.338A>C (p.Glu113Ala)
19g.50210583A>GCA406946203MYH14c.218A>G (p.Glu73Gly)
c.-2073A>G (n.-2073A>G)
c.338A>G (p.Glu113Gly)
 gnomAD v4
19g.50210583A>TCA406946205MYH14c.218A>T (p.Glu73Val)
c.-2073A>T (n.-2073A>T)
c.338A>T (p.Glu113Val)
19g.50210584delCA2586537515MYH14c.219del (p.Gly74AlafsTer26)
c.-2072del (n.-2072del)
c.339del (p.Gly114AlafsTer26)
 gnomAD v4
19g.50210584A>CCA406946207MYH14c.219A>C (p.Glu73Asp)
c.-2072A>C (n.-2072A>C)
c.339A>C (p.Glu113Asp)
19g.50210584A>GCA508302596MYH14c.219A>G (p.Glu73=)
c.-2072A>G (n.-2072A>G)
c.339A>G (p.Glu113=)
 gnomAD v4
19g.50210584A>TCA406946209MYH14c.219A>T (p.Glu73Asp)
c.-2072A>T (n.-2072A>T)
c.339A>T (p.Glu113Asp)
 gnomAD v4
19g.50210585G>ACA406946211MYH14c.220G>A (p.Gly74Ser)
c.-2071G>A (n.-2071G>A)
c.340G>A (p.Gly114Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210585G>CCA406946213MYH14c.220G>C (p.Gly74Arg)
c.-2071G>C (n.-2071G>C)
c.340G>C (p.Gly114Arg)
19g.50210585G=CA2340790503MYH14c.220G= (p.Gly74=)
c.-2071G= (n.-2071G=)
c.340G= (p.Gly114=)
19g.50210585G>TCA406946215MYH14c.220G>T (p.Gly74Cys)
c.-2071G>T (n.-2071G>T)
c.340G>T (p.Gly114Cys)
 gnomAD v4
19g.50210586G>ACA406946219MYH14c.221G>A (p.Gly74Asp)
c.-2070G>A (n.-2070G>A)
c.341G>A (p.Gly114Asp)
 dbSNP gnomAD v2 gnomAD v4
19g.50210586G>CCA406946221MYH14c.221G>C (p.Gly74Ala)
c.-2070G>C (n.-2070G>C)
c.341G>C (p.Gly114Ala)
 gnomAD v4
19g.50210586G=CA2340790504MYH14c.221G= (p.Gly74=)
c.-2070G= (n.-2070G=)
c.341G= (p.Gly114=)
19g.50210586G>TCA406946217MYH14c.221G>T (p.Gly74Val)
c.-2070G>T (n.-2070G>T)
c.341G>T (p.Gly114Val)
 gnomAD v4
19g.50210587C>ACA508302597MYH14c.222C>A (p.Gly74=)
c.-2069C>A (n.-2069C>A)
c.342C>A (p.Gly114=)
 gnomAD v4
19g.50210587C=CA2340790505MYH14c.222C= (p.Gly74=)
c.-2069C= (n.-2069C=)
c.342C= (p.Gly114=)
19g.50210587C>GCA508302598MYH14c.222C>G (p.Gly74=)
c.-2069C>G (n.-2069C>G)
c.342C>G (p.Gly114=)
19g.50210587C>TCA9592211MYH14c.222C>T (p.Gly74=)
c.-2069C>T (n.-2069C>T)
c.342C>T (p.Gly114=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210587_50210590delinsCGAGCA2340790506MYH14c.222_225delinsCGAG (p.Gly74=)
c.-2069_-2066delinsCGAG (n.-2069_-2066delinsCGAG)
c.342_345delinsCGAG (p.Gly114=)
19g.50210588G>ACA9592212MYH14c.223G>A (p.Glu75Lys)
c.-2068G>A (n.-2068G>A)
c.343G>A (p.Glu115Lys)
 dbSNP ExAC gnomAD v4
19g.50210588G>CCA406946224MYH14c.223G>C (p.Glu75Gln)
c.-2068G>C (n.-2068G>C)
c.343G>C (p.Glu115Gln)
 dbSNP gnomAD v2
19g.50210588G=CA2340790508MYH14c.223G= (p.Glu75=)
c.-2068G= (n.-2068G=)
c.343G= (p.Glu115=)
19g.50210588G>TCA406946226MYH14c.223G>T (p.Glu75Ter)
c.-2068G>T (n.-2068G>T)
c.343G>T (p.Glu115Ter)
 gnomAD v4
19g.50210595_50210597delCA2340790507MYH14c.230_232del (p.Glu77del)
c.-2061_-2059del (n.-2061_-2059del)
c.350_352del (p.Glu117del)
 dbSNP
19g.50210589A>CCA406946227MYH14c.224A>C (p.Glu75Ala)
c.-2067A>C (n.-2067A>C)
c.344A>C (p.Glu115Ala)
19g.50210589A>GCA406946229MYH14c.224A>G (p.Glu75Gly)
c.-2067A>G (n.-2067A>G)
c.344A>G (p.Glu115Gly)
 gnomAD v4
19g.50210589A>TCA406946231MYH14c.224A>T (p.Glu75Val)
c.-2067A>T (n.-2067A>T)
c.344A>T (p.Glu115Val)
19g.50210590G>ACA508302599MYH14c.225G>A (p.Glu75=)
c.-2066G>A (n.-2066G>A)
c.345G>A (p.Glu115=)
 gnomAD v4
19g.50210590G>CCA406946233MYH14c.225G>C (p.Glu75Asp)
c.-2066G>C (n.-2066G>C)
c.345G>C (p.Glu115Asp)
19g.50210590G>TCA406946235MYH14c.225G>T (p.Glu75Asp)
c.-2066G>T (n.-2066G>T)
c.345G>T (p.Glu115Asp)
 gnomAD v4
19g.50210591G>ACA406946237MYH14c.226G>A (p.Glu76Lys)
c.-2065G>A (n.-2065G>A)
c.346G>A (p.Glu116Lys)
 dbSNP gnomAD v2 gnomAD v4
19g.50210591G>CCA406946238MYH14c.226G>C (p.Glu76Gln)
c.-2065G>C (n.-2065G>C)
c.346G>C (p.Glu116Gln)
19g.50210591G=CA2340790509MYH14c.226G= (p.Glu76=)
c.-2065G= (n.-2065G=)
c.346G= (p.Glu116=)
19g.50210591G>TCA406946240MYH14c.226G>T (p.Glu76Ter)
c.-2065G>T (n.-2065G>T)
c.346G>T (p.Glu116Ter)
 gnomAD v4
19g.50210592A>CCA406946244MYH14c.227A>C (p.Glu76Ala)
c.-2064A>C (n.-2064A>C)
c.347A>C (p.Glu116Ala)
19g.50210592A>GCA406946246MYH14c.227A>G (p.Glu76Gly)
c.-2064A>G (n.-2064A>G)
c.347A>G (p.Glu116Gly)
19g.50210592A>TCA406946243MYH14c.227A>T (p.Glu76Val)
c.-2064A>T (n.-2064A>T)
c.347A>T (p.Glu116Val)
19g.50210593G>ACA508302600MYH14c.228G>A (p.Glu76=)
c.-2063G>A (n.-2063G>A)
c.348G>A (p.Glu116=)
 gnomAD v4
19g.50210593G>CCA406946248MYH14c.228G>C (p.Glu76Asp)
c.-2063G>C (n.-2063G>C)
c.348G>C (p.Glu116Asp)
19g.50210593G>TCA406946249MYH14c.228G>T (p.Glu76Asp)
c.-2063G>T (n.-2063G>T)
c.348G>T (p.Glu116Asp)
 gnomAD v4
19g.50210594G>ACA406946252MYH14c.229G>A (p.Glu77Lys)
c.-2062G>A (n.-2062G>A)
c.349G>A (p.Glu117Lys)
 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210594G>CCA406946253MYH14c.229G>C (p.Glu77Gln)
c.-2062G>C (n.-2062G>C)
c.349G>C (p.Glu117Gln)
19g.50210594G>TCA406946255MYH14c.229G>T (p.Glu77Ter)
c.-2062G>T (n.-2062G>T)
c.349G>T (p.Glu117Ter)
 gnomAD v4
19g.50210595A=CA2340790510MYH14c.230A= (p.Glu77=)
c.-2061A= (n.-2061A=)
c.350A= (p.Glu117=)
19g.50210595A>CCA9592213MYH14c.230A>C (p.Glu77Ala)
c.-2061A>C (n.-2061A>C)
c.350A>C (p.Glu117Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210595A>GCA406946257MYH14c.230A>G (p.Glu77Gly)
c.-2061A>G (n.-2061A>G)
c.350A>G (p.Glu117Gly)
 gnomAD v4
19g.50210595A>TCA406946259MYH14c.230A>T (p.Glu77Val)
c.-2061A>T (n.-2061A>T)
c.350A>T (p.Glu117Val)
19g.50210596G>ACA508302601MYH14c.231G>A (p.Glu77=)
c.-2060G>A (n.-2060G>A)
c.351G>A (p.Glu117=)
 gnomAD v4
19g.50210596G>CCA406946262MYH14c.231G>C (p.Glu77Asp)
c.-2060G>C (n.-2060G>C)
c.351G>C (p.Glu117Asp)
19g.50210596G>TCA406946264MYH14c.231G>T (p.Glu77Asp)
c.-2060G>T (n.-2060G>T)
c.351G>T (p.Glu117Asp)
 gnomAD v4
19g.50210597G>ACA406946266MYH14c.232G>A (p.Ala78Thr)
c.-2059G>A (n.-2059G>A)
c.352G>A (p.Ala118Thr)
 gnomAD v4
19g.50210597G>CCA406946268MYH14c.232G>C (p.Ala78Pro)
c.-2059G>C (n.-2059G>C)
c.352G>C (p.Ala118Pro)
19g.50210597G=CA2340790511MYH14c.232G= (p.Ala78=)
c.-2059G= (n.-2059G=)
c.352G= (p.Ala118=)
19g.50210597G>TCA406946269MYH14c.232G>T (p.Ala78Ser)
c.-2059G>T (n.-2059G>T)
c.352G>T (p.Ala118Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210598C>ACA406946274MYH14c.233C>A (p.Ala78Glu)
c.-2058C>A (n.-2058C>A)
c.353C>A (p.Ala118Glu)
 gnomAD v4
19g.50210598C=CA2340790512MYH14c.233C= (p.Ala78=)
c.-2058C= (n.-2058C=)
c.353C= (p.Ala118=)
19g.50210598C>GCA406946272MYH14c.233C>G (p.Ala78Gly)
c.-2058C>G (n.-2058C>G)
c.353C>G (p.Ala118Gly)
19g.50210598C>TCA9592214MYH14c.233C>T (p.Ala78Val)
c.-2058C>T (n.-2058C>T)
c.353C>T (p.Ala118Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.50210599G>ACA309565529MYH14c.234G>A (p.Ala78=)
c.-2057G>A (n.-2057G>A)
c.354G>A (p.Ala118=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.50210599G>CCA508302603MYH14c.234G>C (p.Ala78=)
c.-2057G>C (n.-2057G>C)
c.354G>C (p.Ala118=)
 gnomAD v4
19g.50210599G=CA2340790513MYH14c.234G= (p.Ala78=)
c.-2057G= (n.-2057G=)
c.354G= (p.Ala118=)
19g.50210599G>TCA508302602MYH14c.234G>T (p.Ala78=)
c.-2057G>T (n.-2057G>T)
c.354G>T (p.Ala118=)
 dbSNP gnomAD v2 gnomAD v4
19g.50210603_50210608delCA2697556652MYH14c.238_243del (p.Val80_Glu81del)
c.-2053_-2048del (n.-2053_-2048del)
c.358_363del (p.Val120_Glu121del)
 ClinVar
19g.50210600G>ACA406946276MYH14c.235G>A (p.Glu79Lys)
c.-2056G>A (n.-2056G>A)
c.355G>A (p.Glu119Lys)
19g.50210600G>CCA406946278MYH14c.235G>C (p.Glu79Gln)
c.-2056G>C (n.-2056G>C)
c.355G>C (p.Glu119Gln)
19g.50210600G>TCA406946279MYH14c.235G>T (p.Glu79Ter)
c.-2056G>T (n.-2056G>T)
c.355G>T (p.Glu119Ter)
 gnomAD v4
19g.50210601A=CA2340790514MYH14c.236A= (p.Glu79=)
c.-2055A= (n.-2055A=)
c.356A= (p.Glu119=)
19g.50210601A>CCA406946282MYH14c.236A>C (p.Glu79Ala)
c.-2055A>C (n.-2055A>C)
c.356A>C (p.Glu119Ala)
19g.50210601A>GCA309565543MYH14c.236A>G (p.Glu79Gly)
c.-2055A>G (n.-2055A>G)
c.356A>G (p.Glu119Gly)
 dbSNP gnomAD v3 gnomAD v4
19g.50210601A>TCA9592215MYH14c.236A>T (p.Glu79Val)
c.-2055A>T (n.-2055A>T)
c.356A>T (p.Glu119Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.50210602G>ACA508302604MYH14c.237G>A (p.Glu79=)
c.-2054G>A (n.-2054G>A)
c.357G>A (p.Glu119=)
 dbSNP gnomAD v4
19g.50210602G>CCA406946287MYH14c.237G>C (p.Glu79Asp)
c.-2054G>C (n.-2054G>C)
c.357G>C (p.Glu119Asp)
19g.50210602G=CA2340790515MYH14c.237G= (p.Glu79=)
c.-2054G= (n.-2054G=)
c.357G= (p.Glu119=)
19g.50210602G>TCA406946285MYH14c.237G>T (p.Glu79Asp)
c.-2054G>T (n.-2054G>T)
c.357G>T (p.Glu119Asp)
 gnomAD v4
19g.50210603G>ACA406946289MYH14c.238G>A (p.Val80Met)
c.-2053G>A (n.-2053G>A)
c.358G>A (p.Val120Met)
19g.50210603G>CCA406946291MYH14c.238G>C (p.Val80Leu)
c.-2053G>C (n.-2053G>C)
c.358G>C (p.Val120Leu)
19g.50210603G=CA2340790516MYH14c.238G= (p.Val80=)
c.-2053G= (n.-2053G=)
c.358G= (p.Val120=)
19g.50210603G>TCA406946292MYH14c.238G>T (p.Val80Leu)
c.-2053G>T (n.-2053G>T)
c.358G>T (p.Val120Leu)
 gnomAD v4
19g.50210604T>ACA406946294MYH14c.239T>A (p.Val80Glu)
c.-2052T>A (n.-2052T>A)
c.359T>A (p.Val120Glu)
19g.50210604T>CCA406946295MYH14c.239T>C (p.Val80Ala)
c.-2052T>C (n.-2052T>C)
c.359T>C (p.Val120Ala)
 COSMIC COSMIC
19g.50210604T>GCA406946296MYH14c.239T>G (p.Val80Gly)
c.-2052T>G (n.-2052T>G)
c.359T>G (p.Val120Gly)
 dbSNP
19g.50210604T=CA2340790517MYH14c.239T= (p.Val80=)
c.-2052T= (n.-2052T=)
c.359T= (p.Val120=)
19g.50210607_50210612dupCA633896634MYH14c.242_247dup (p.Leu82_Ala83insGluLeu)
c.-2049_-2044dup (n.-2049_-2044dup)
c.362_367dup (p.Leu122_Ala123insGluLeu)
 dbSNP gnomAD v2 gnomAD v4
19g.50210605G>ACA508302605MYH14c.240G>A (p.Val80=)
c.-2051G>A (n.-2051G>A)
c.360G>A (p.Val120=)
 gnomAD v4
19g.50210605G>CCA508302607MYH14c.240G>C (p.Val80=)
c.-2051G>C (n.-2051G>C)
c.360G>C (p.Val120=)
19g.50210605G>TCA508302606MYH14c.240G>T (p.Val80=)
c.-2051G>T (n.-2051G>T)
c.360G>T (p.Val120=)
 gnomAD v4
19g.50210606G>ACA406946300MYH14c.241G>A (p.Glu81Lys)
c.-2050G>A (n.-2050G>A)
c.361G>A (p.Glu121Lys)
 dbSNP gnomAD v4
19g.50210606G>CCA406946297MYH14c.241G>C (p.Glu81Gln)
c.-2050G>C (n.-2050G>C)
c.361G>C (p.Glu121Gln)
19g.50210606G>TCA406946299MYH14c.241G>T (p.Glu81Ter)
c.-2050G>T (n.-2050G>T)
c.361G>T (p.Glu121Ter)
 gnomAD v4
19g.50210607A>CCA406946304MYH14c.242A>C (p.Glu81Ala)
c.-2049A>C (n.-2049A>C)
c.362A>C (p.Glu121Ala)
19g.50210607A>GCA406946305MYH14c.242A>G (p.Glu81Gly)
c.-2049A>G (n.-2049A>G)
c.362A>G (p.Glu121Gly)
 gnomAD v4
19g.50210607A>TCA406946307MYH14c.242A>T (p.Glu81Val)
c.-2049A>T (n.-2049A>T)
c.362A>T (p.Glu121Val)
19g.50210608G>ACA508302608MYH14c.243G>A (p.Glu81=)
c.-2048G>A (n.-2048G>A)
c.363G>A (p.Glu121=)
 dbSNP gnomAD v4
19g.50210608G>CCA406946309MYH14c.243G>C (p.Glu81Asp)
c.-2048G>C (n.-2048G>C)
c.363G>C (p.Glu121Asp)
19g.50210608G=CA2340790518MYH14c.243G= (p.Glu81=)
c.-2048G= (n.-2048G=)
c.363G= (p.Glu121=)
19g.50210608G>TCA309565559MYH14c.243G>T (p.Glu81Asp)
c.-2048G>T (n.-2048G>T)
c.363G>T (p.Glu121Asp)
 ClinVar dbSNP gnomAD v4
19g.50210609C>ACA406946312MYH14c.244C>A (p.Leu82Met)
c.-2047C>A (n.-2047C>A)
c.364C>A (p.Leu122Met)
 gnomAD v4
19g.50210609C>GCA406946313MYH14c.244C>G (p.Leu82Val)
c.-2047C>G (n.-2047C>G)
c.364C>G (p.Leu122Val)
19g.50210609C>TCA508175167MYH14c.244C>T (p.Leu82=)
c.-2047C>T (n.-2047C>T)
c.364C>T (p.Leu122=)
 gnomAD v4
19g.50210610T>ACA406946316MYH14c.245T>A (p.Leu82Gln)
c.-2046T>A (n.-2046T>A)
c.365T>A (p.Leu122Gln)
19g.50210610T>CCA406946318MYH14c.245T>C (p.Leu82Pro)
c.-2046T>C (n.-2046T>C)
c.365T>C (p.Leu122Pro)
 gnomAD v4
19g.50210610T>GCA406946319MYH14c.245T>G (p.Leu82Arg)
c.-2046T>G (n.-2046T>G)
c.365T>G (p.Leu122Arg)
19g.50210611G>ACA508175168MYH14c.246G>A (p.Leu82=)
c.-2045G>A (n.-2045G>A)
c.366G>A (p.Leu122=)
 gnomAD v4
19g.50210611G>CCA508175170MYH14c.246G>C (p.Leu82=)
c.-2045G>C (n.-2045G>C)
c.366G>C (p.Leu122=)
19g.50210611G>TCA508175172MYH14c.246G>T (p.Leu82=)
c.-2045G>T (n.-2045G>T)
c.366G>T (p.Leu122=)
 gnomAD v4
19g.50210612G>ACA406946322MYH14c.247G>A (p.Ala83Thr)
c.-2044G>A (n.-2044G>A)
c.367G>A (p.Ala123Thr)
 dbSNP gnomAD v2 gnomAD v4
19g.50210612G>CCA406946324MYH14c.247G>C (p.Ala83Pro)
c.-2044G>C (n.-2044G>C)
c.367G>C (p.Ala123Pro)
19g.50210612G=CA2340790519MYH14c.247G= (p.Ala83=)
c.-2044G= (n.-2044G=)
c.367G= (p.Ala123=)
19g.50210612G>TCA406946326MYH14c.247G>T (p.Ala83Ser)
c.-2044G>T (n.-2044G>T)
c.367G>T (p.Ala123Ser)
 gnomAD v4
19g.50210613C>ACA406946328MYH14c.248C>A (p.Ala83Glu)
c.-2043C>A (n.-2043C>A)
c.368C>A (p.Ala123Glu)
 dbSNP gnomAD v2 gnomAD v4
19g.50210613C=CA2340790520MYH14c.248C= (p.Ala83=)
c.-2043C= (n.-2043C=)
c.368C= (p.Ala123=)
19g.50210613C>GCA406946332MYH14c.248C>G (p.Ala83Gly)
c.-2043C>G (n.-2043C>G)
c.368C>G (p.Ala123Gly)
19g.50210613C>TCA406946330MYH14c.248C>T (p.Ala83Val)
c.-2043C>T (n.-2043C>T)
c.368C>T (p.Ala123Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210614G>ACA309565569MYH14c.249G>A (p.Ala83=)
c.-2042G>A (n.-2042G>A)
c.369G>A (p.Ala123=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210614G>CCA508175177MYH14c.249G>C (p.Ala83=)
c.-2042G>C (n.-2042G>C)
c.369G>C (p.Ala123=)
19g.50210614G=CA2340790521MYH14c.249G= (p.Ala83=)
c.-2042G= (n.-2042G=)
c.369G= (p.Ala123=)
19g.50210614G>TCA508175178MYH14c.249G>T (p.Ala83=)
c.-2042G>T (n.-2042G>T)
c.369G>T (p.Ala123=)
 gnomAD v4
19g.50210615G>ACA406946334MYH14c.250G>A (p.Glu84Lys)
c.-2041G>A (n.-2041G>A)
c.370G>A (p.Glu124Lys)
19g.50210615G>CCA406946335MYH14c.250G>C (p.Glu84Gln)
c.-2041G>C (n.-2041G>C)
c.370G>C (p.Glu124Gln)
19g.50210615G>TCA406946337MYH14c.250G>T (p.Glu84Ter)
c.-2041G>T (n.-2041G>T)
c.370G>T (p.Glu124Ter)
19g.50210616A>CCA406946339MYH14c.251A>C (p.Glu84Ala)
c.-2040A>C (n.-2040A>C)
c.371A>C (p.Glu124Ala)
19g.50210616A>GCA406946341MYH14c.251A>G (p.Glu84Gly)
c.-2040A>G (n.-2040A>G)
c.371A>G (p.Glu124Gly)
 gnomAD v4
19g.50210616A>TCA406946342MYH14c.251A>T (p.Glu84Val)
c.-2040A>T (n.-2040A>T)
c.371A>T (p.Glu124Val)
19g.50210617delCA2586537516MYH14c.252del (p.Ser85AlafsTer15)
c.-2039del (n.-2039del)
c.372del (p.Ser125AlafsTer15)
 gnomAD v4
19g.50210617G>ACA508175179MYH14c.252G>A (p.Glu84=)
c.-2039G>A (n.-2039G>A)
c.372G>A (p.Glu124=)
 gnomAD v4
19g.50210617G>CCA406946345MYH14c.252G>C (p.Glu84Asp)
c.-2039G>C (n.-2039G>C)
c.372G>C (p.Glu124Asp)
19g.50210617G>TCA406946347MYH14c.252G>T (p.Glu84Asp)
c.-2039G>T (n.-2039G>T)
c.372G>T (p.Glu124Asp)
 gnomAD v4
19g.50210618A>CCA406946349MYH14c.253A>C (p.Ser85Arg)
c.-2038A>C (n.-2038A>C)
c.373A>C (p.Ser125Arg)
19g.50210618A>GCA406946351MYH14c.253A>G (p.Ser85Gly)
c.-2038A>G (n.-2038A>G)
c.373A>G (p.Ser125Gly)
19g.50210618A>TCA406946353MYH14c.253A>T (p.Ser85Cys)
c.-2038A>T (n.-2038A>T)
c.373A>T (p.Ser125Cys)
19g.50210619G>ACA406946359MYH14c.254G>A (p.Ser85Asn)
c.-2037G>A (n.-2037G>A)
c.374G>A (p.Ser125Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.50210619G>CCA406946355MYH14c.254G>C (p.Ser85Thr)
c.-2037G>C (n.-2037G>C)
c.374G>C (p.Ser125Thr)
19g.50210619G=CA2340790522MYH14c.254G= (p.Ser85=)
c.-2037G= (n.-2037G=)
c.374G= (p.Ser125=)
19g.50210619G>TCA406946357MYH14c.254G>T (p.Ser85Ile)
c.-2037G>T (n.-2037G>T)
c.374G>T (p.Ser125Ile)
 gnomAD v4
19g.50210620C>ACA406946360MYH14c.255C>A (p.Ser85Arg)
c.-2036C>A (n.-2036C>A)
c.375C>A (p.Ser125Arg)
 gnomAD v4
19g.50210620C=CA2340790523MYH14c.255C= (p.Ser85=)
c.-2036C= (n.-2036C=)
c.375C= (p.Ser125=)
19g.50210620C>GCA406946361MYH14c.255C>G (p.Ser85Arg)
c.-2036C>G (n.-2036C>G)
c.375C>G (p.Ser125Arg)
 dbSNP
19g.50210620C>TCA508175183MYH14c.255C>T (p.Ser85=)
c.-2036C>T (n.-2036C>T)
c.375C>T (p.Ser125=)
 dbSNP gnomAD v2 gnomAD v4
19g.50210621G>ACA406946363MYH14c.256G>A (p.Gly86Arg)
c.-2035G>A (n.-2035G>A)
c.376G>A (p.Gly126Arg)
 dbSNP gnomAD v4
19g.50210621G>CCA406946365MYH14c.256G>C (p.Gly86Arg)
c.-2035G>C (n.-2035G>C)
c.376G>C (p.Gly126Arg)
 gnomAD v4
19g.50210621G=CA2340790524MYH14c.256G= (p.Gly86=)
c.-2035G= (n.-2035G=)
c.376G= (p.Gly126=)
19g.50210621G>TCA406946367MYH14c.256G>T (p.Gly86Trp)
c.-2035G>T (n.-2035G>T)
c.376G>T (p.Gly126Trp)
 gnomAD v4
19g.50210622G>ACA406946369MYH14c.257G>A (p.Gly86Glu)
c.-2034G>A (n.-2034G>A)
c.377G>A (p.Gly126Glu)
19g.50210622G>CCA406946371MYH14c.257G>C (p.Gly86Ala)
c.-2034G>C (n.-2034G>C)
c.377G>C (p.Gly126Ala)
19g.50210622G>TCA406946373MYH14c.257G>T (p.Gly86Val)
c.-2034G>T (n.-2034G>T)
c.377G>T (p.Gly126Val)
 gnomAD v4
19g.50210623G>ACA9592216MYH14c.258G>A (p.Gly86=)
c.-2033G>A (n.-2033G>A)
c.378G>A (p.Gly126=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210623G>CCA508175187MYH14c.258G>C (p.Gly86=)
c.-2033G>C (n.-2033G>C)
c.378G>C (p.Gly126=)
19g.50210623G=CA2340790525MYH14c.258G= (p.Gly86=)
c.-2033G= (n.-2033G=)
c.378G= (p.Gly126=)
19g.50210623G>TCA508175188MYH14c.258G>T (p.Gly86=)
c.-2033G>T (n.-2033G>T)
c.378G>T (p.Gly126=)
 gnomAD v4
19g.50210624A>CCA508175190MYH14c.259A>C (p.Arg87=)
c.-2032A>C (n.-2032A>C)
c.379A>C (p.Arg127=)
19g.50210624A>GCA406946376MYH14c.259A>G (p.Arg87Gly)
c.-2032A>G (n.-2032A>G)
c.379A>G (p.Arg127Gly)
19g.50210624A>TCA406946377MYH14c.259A>T (p.Arg87Trp)
c.-2032A>T (n.-2032A>T)
c.379A>T (p.Arg127Trp)
 gnomAD v4
19g.50210625G>ACA406946383MYH14c.260G>A (p.Arg87Lys)
c.-2031G>A (n.-2031G>A)
c.380G>A (p.Arg127Lys)
 gnomAD v4
19g.50210625G>CCA406946382MYH14c.260G>C (p.Arg87Thr)
c.-2031G>C (n.-2031G>C)
c.380G>C (p.Arg127Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.50210625G=CA2340790526MYH14c.260G= (p.Arg87=)
c.-2031G= (n.-2031G=)
c.380G= (p.Arg127=)
19g.50210625G>TCA406946380MYH14c.260G>T (p.Arg87Met)
c.-2031G>T (n.-2031G>T)
c.380G>T (p.Arg127Met)
 gnomAD v4
19g.50210626G>ACA508175192MYH14c.261G>A (p.Arg87=)
c.-2030G>A (n.-2030G>A)
c.381G>A (p.Arg127=)
19g.50210626G>CCA406946386MYH14c.261G>C (p.Arg87Ser)
c.-2030G>C (n.-2030G>C)
c.381G>C (p.Arg127Ser)
19g.50210626G>TCA406946388MYH14c.261G>T (p.Arg87Ser)
c.-2030G>T (n.-2030G>T)
c.381G>T (p.Arg127Ser)
 gnomAD v4
19g.50210627C>ACA508175193MYH14c.262C>A (p.Arg88=)
c.-2029C>A (n.-2029C>A)
c.382C>A (p.Arg128=)
 gnomAD v4
19g.50210627C=CA2340790527MYH14c.262C= (p.Arg88=)
c.-2029C= (n.-2029C=)
c.382C= (p.Arg128=)
19g.50210627C>GCA406946390MYH14c.262C>G (p.Arg88Gly)
c.-2029C>G (n.-2029C>G)
c.382C>G (p.Arg128Gly)
19g.50210627C>TCA9592217MYH14c.262C>T (p.Arg88Trp)
c.-2029C>T (n.-2029C>T)
c.382C>T (p.Arg128Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210628G>ACA9592218MYH14c.263G>A (p.Arg88Gln)
c.-2028G>A (n.-2028G>A)
c.383G>A (p.Arg128Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210628G>CCA406946394MYH14c.263G>C (p.Arg88Pro)
c.-2028G>C (n.-2028G>C)
c.383G>C (p.Arg128Pro)
 gnomAD v4
19g.50210628G=CA2340790528MYH14c.263G= (p.Arg88=)
c.-2028G= (n.-2028G=)
c.383G= (p.Arg128=)
19g.50210628G>TCA406946396MYH14c.263G>T (p.Arg88Leu)
c.-2028G>T (n.-2028G>T)
c.383G>T (p.Arg128Leu)
 gnomAD v4
19g.50210628_50210635dupCA2586537517MYH14c.263_270dup (p.Leu91GlyfsTer12)
c.-2028_-2021dup (n.-2028_-2021dup)
c.383_390dup (p.Leu131GlyfsTer12)
 gnomAD v4
19g.50210629G>ACA508175195MYH14c.264G>A (p.Arg88=)
c.-2027G>A (n.-2027G>A)
c.384G>A (p.Arg128=)
 gnomAD v4
19g.50210629G>CCA508175196MYH14c.264G>C (p.Arg88=)
c.-2027G>C (n.-2027G>C)
c.384G>C (p.Arg128=)
19g.50210629G>TCA508175197MYH14c.264G>T (p.Arg88=)
c.-2027G>T (n.-2027G>T)
c.384G>T (p.Arg128=)
 gnomAD v4
19g.50210630C>ACA406946398MYH14c.265C>A (p.Leu89Met)
c.-2026C>A (n.-2026C>A)
c.385C>A (p.Leu129Met)
 gnomAD v4
19g.50210630C=CA2340790529MYH14c.265C= (p.Leu89=)
c.-2026C= (n.-2026C=)
c.385C= (p.Leu129=)
19g.50210630C>GCA406946400MYH14c.265C>G (p.Leu89Val)
c.-2026C>G (n.-2026C>G)
c.385C>G (p.Leu129Val)
19g.50210630C>TCA508175198MYH14c.265C>T (p.Leu89=)
c.-2026C>T (n.-2026C>T)
c.385C>T (p.Leu129=)
 dbSNP gnomAD v3 gnomAD v4
19g.50210631T>ACA406946402MYH14c.266T>A (p.Leu89Gln)
c.-2025T>A (n.-2025T>A)
c.386T>A (p.Leu129Gln)
19g.50210631T>CCA309565589MYH14c.266T>C (p.Leu89Pro)
c.-2025T>C (n.-2025T>C)
c.386T>C (p.Leu129Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210631T>GCA406946403MYH14c.266T>G (p.Leu89Arg)
c.-2025T>G (n.-2025T>G)
c.386T>G (p.Leu129Arg)
19g.50210631T=CA2340790530MYH14c.266T= (p.Leu89=)
c.-2025T= (n.-2025T=)
c.386T= (p.Leu129=)

Number of alleles fetched