Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.50210628_50210635dupCA2586537517MYH14c.263_270dup (p.Leu91GlyfsTer12)
c.-2028_-2021dup (n.-2028_-2021dup)
c.383_390dup (p.Leu131GlyfsTer12)
 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=)
19g.50210632G>ACA508175199MYH14c.267G>A (p.Leu89=)
c.-2024G>A (n.-2024G>A)
c.387G>A (p.Leu129=)
 gnomAD v4
19g.50210632G>CCA508175203MYH14c.267G>C (p.Leu89=)
c.-2024G>C (n.-2024G>C)
c.387G>C (p.Leu129=)
19g.50210632G>TCA508175201MYH14c.267G>T (p.Leu89=)
c.-2024G>T (n.-2024G>T)
c.387G>T (p.Leu129=)
19g.50210633C>ACA508175205MYH14c.268C>A (p.Arg90=)
c.-2023C>A (n.-2023C>A)
c.388C>A (p.Arg130=)
 gnomAD v4
19g.50210633C>GCA406946406MYH14c.268C>G (p.Arg90Gly)
c.-2023C>G (n.-2023C>G)
c.388C>G (p.Arg130Gly)
19g.50210633C>TCA406946407MYH14c.268C>T (p.Arg90Ter)
c.-2023C>T (n.-2023C>T)
c.388C>T (p.Arg130Ter)
 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210634G>ACA309565593MYH14c.269G>A (p.Arg90Gln)
c.-2022G>A (n.-2022G>A)
c.389G>A (p.Arg130Gln)
 dbSNP gnomAD v2 gnomAD v4
19g.50210634G>CCA406946410MYH14c.269G>C (p.Arg90Pro)
c.-2022G>C (n.-2022G>C)
c.389G>C (p.Arg130Pro)
 dbSNP gnomAD v4
19g.50210634G=CA2340790531MYH14c.269G= (p.Arg90=)
c.-2022G= (n.-2022G=)
c.389G= (p.Arg130=)
19g.50210634G>TCA406946412MYH14c.269G>T (p.Arg90Leu)
c.-2022G>T (n.-2022G>T)
c.389G>T (p.Arg130Leu)
 gnomAD v4
19g.50210635A>CCA508175206MYH14c.270A>C (p.Arg90=)
c.-2021A>C (n.-2021A>C)
c.390A>C (p.Arg130=)
19g.50210635A>GCA508175207MYH14c.270A>G (p.Arg90=)
c.-2021A>G (n.-2021A>G)
c.390A>G (p.Arg130=)
19g.50210635A>TCA508175209MYH14c.270A>T (p.Arg90=)
c.-2021A>T (n.-2021A>T)
c.390A>T (p.Arg130=)
19g.50210636C>ACA406946414MYH14c.271C>A (p.Leu91Met)
c.-2020C>A (n.-2020C>A)
c.391C>A (p.Leu131Met)
19g.50210636C>GCA406946416MYH14c.271C>G (p.Leu91Val)
c.-2020C>G (n.-2020C>G)
c.391C>G (p.Leu131Val)
19g.50210636C>TCA508175210MYH14c.271C>T (p.Leu91=)
c.-2020C>T (n.-2020C>T)
c.391C>T (p.Leu131=)
 gnomAD v4
19g.50210637T>ACA406946418MYH14c.272T>A (p.Leu91Gln)
c.-2019T>A (n.-2019T>A)
c.392T>A (p.Leu131Gln)
19g.50210637T>CCA406946420MYH14c.272T>C (p.Leu91Pro)
c.-2019T>C (n.-2019T>C)
c.392T>C (p.Leu131Pro)
19g.50210637T>GCA406946422MYH14c.272T>G (p.Leu91Arg)
c.-2019T>G (n.-2019T>G)
c.392T>G (p.Leu131Arg)
19g.50210638G>ACA508175212MYH14c.273G>A (p.Leu91=)
c.-2018G>A (n.-2018G>A)
c.393G>A (p.Leu131=)
 gnomAD v4
19g.50210638G>CCA508175214MYH14c.273G>C (p.Leu91=)
c.-2018G>C (n.-2018G>C)
c.393G>C (p.Leu131=)
19g.50210638G>TCA508175216MYH14c.273G>T (p.Leu91=)
c.-2018G>T (n.-2018G>T)
c.393G>T (p.Leu131=)
 gnomAD v4
19g.50210639C>ACA406946424MYH14c.274C>A (p.Pro92Thr)
c.-2017C>A (n.-2017C>A)
c.394C>A (p.Pro132Thr)
 dbSNP gnomAD v2 gnomAD v4
19g.50210639C=CA2340790532MYH14c.274C= (p.Pro92=)
c.-2017C= (n.-2017C=)
c.394C= (p.Pro132=)
19g.50210639C>GCA406946426MYH14c.274C>G (p.Pro92Ala)
c.-2017C>G (n.-2017C>G)
c.394C>G (p.Pro132Ala)
19g.50210639C>TCA406946427MYH14c.274C>T (p.Pro92Ser)
c.-2017C>T (n.-2017C>T)
c.394C>T (p.Pro132Ser)
 gnomAD v4
19g.50210640C>ACA406946428MYH14c.275C>A (p.Pro92Gln)
c.-2016C>A (n.-2016C>A)
c.395C>A (p.Pro132Gln)
 gnomAD v4
19g.50210640C=CA2340790533MYH14c.275C= (p.Pro92=)
c.-2016C= (n.-2016C=)
c.395C= (p.Pro132=)
19g.50210640C>GCA406946430MYH14c.275C>G (p.Pro92Arg)
c.-2016C>G (n.-2016C>G)
c.395C>G (p.Pro132Arg)
 gnomAD v4
19g.50210640C>TCA9592219MYH14c.275C>T (p.Pro92Leu)
c.-2016C>T (n.-2016C>T)
c.395C>T (p.Pro132Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.50210641G>ACA309565603MYH14c.276G>A (p.Pro92=)
c.-2015G>A (n.-2015G>A)
c.396G>A (p.Pro132=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.50210641G>CCA508175218MYH14c.276G>C (p.Pro92=)
c.-2015G>C (n.-2015G>C)
c.396G>C (p.Pro132=)
 dbSNP gnomAD v2 gnomAD v4
19g.50210641G=CA2340790534MYH14c.276G= (p.Pro92=)
c.-2015G= (n.-2015G=)
c.396G= (p.Pro132=)
19g.50210641G>TCA508175219MYH14c.276G>T (p.Pro92=)
c.-2015G>T (n.-2015G>T)
c.396G>T (p.Pro132=)
 gnomAD v4
19g.50210642C>ACA508175220MYH14c.277C>A (p.Arg93=)
c.-2014C>A (n.-2014C>A)
c.397C>A (p.Arg133=)
 gnomAD v4
19g.50210642C=CA2340790535MYH14c.277C= (p.Arg93=)
c.-2014C= (n.-2014C=)
c.397C= (p.Arg133=)
19g.50210642C>GCA406946433MYH14c.277C>G (p.Arg93Gly)
c.-2014C>G (n.-2014C>G)
c.397C>G (p.Arg133Gly)
 gnomAD v4
19g.50210642C>TCA406946435MYH14c.277C>T (p.Arg93Trp)
c.-2014C>T (n.-2014C>T)
c.397C>T (p.Arg133Trp)
 dbSNP gnomAD v4
19g.50210643G>ACA406946437MYH14c.278G>A (p.Arg93Gln)
c.-2013G>A (n.-2013G>A)
c.398G>A (p.Arg133Gln)
 gnomAD v4
19g.50210643G>CCA406946439MYH14c.278G>C (p.Arg93Pro)
c.-2013G>C (n.-2013G>C)
c.398G>C (p.Arg133Pro)
19g.50210643G=CA2340790536MYH14c.278G= (p.Arg93=)
c.-2013G= (n.-2013G=)
c.398G= (p.Arg133=)
19g.50210643G>TCA9592220MYH14c.278G>T (p.Arg93Leu)
c.-2013G>T (n.-2013G>T)
c.398G>T (p.Arg133Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210644G>ACA309565621MYH14c.279G>A (p.Arg93=)
c.-2012G>A (n.-2012G>A)
c.399G>A (p.Arg133=)
 dbSNP gnomAD v4
19g.50210644G>CCA9592221MYH14c.279G>C (p.Arg93=)
c.-2012G>C (n.-2012G>C)
c.399G>C (p.Arg133=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210644G=CA2340790537MYH14c.279G= (p.Arg93=)
c.-2012G= (n.-2012G=)
c.399G= (p.Arg133=)
19g.50210644G>TCA508175222MYH14c.279G>T (p.Arg93=)
c.-2012G>T (n.-2012G>T)
c.399G>T (p.Arg133=)
19g.50210645G>ACA406946444MYH14c.280G>A (p.Asp94Asn)
c.-2011G>A (n.-2011G>A)
c.400G>A (p.Asp134Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.50210645G>CCA406946445MYH14c.280G>C (p.Asp94His)
c.-2011G>C (n.-2011G>C)
c.400G>C (p.Asp134His)
19g.50210645G=CA2340790538MYH14c.280G= (p.Asp94=)
c.-2011G= (n.-2011G=)
c.400G= (p.Asp134=)
19g.50210645G>TCA406946447MYH14c.280G>T (p.Asp94Tyr)
c.-2011G>T (n.-2011G>T)
c.400G>T (p.Asp134Tyr)
 gnomAD v4
19g.50210646A>CCA406946450MYH14c.281A>C (p.Asp94Ala)
c.-2010A>C (n.-2010A>C)
c.401A>C (p.Asp134Ala)
19g.50210646A>GCA406946451MYH14c.281A>G (p.Asp94Gly)
c.-2010A>G (n.-2010A>G)
c.401A>G (p.Asp134Gly)
 gnomAD v4
19g.50210646A>TCA406946453MYH14c.281A>T (p.Asp94Val)
c.-2010A>T (n.-2010A>T)
c.401A>T (p.Asp134Val)
19g.50210647C>ACA406946455MYH14c.282C>A (p.Asp94Glu)
c.-2009C>A (n.-2009C>A)
c.402C>A (p.Asp134Glu)
19g.50210647C>GCA406946457MYH14c.282C>G (p.Asp94Glu)
c.-2009C>G (n.-2009C>G)
c.402C>G (p.Asp134Glu)
19g.50210647C>TCA508175226MYH14c.282C>T (p.Asp94=)
c.-2009C>T (n.-2009C>T)
c.402C>T (p.Asp134=)
 gnomAD v4
19g.50210648C>ACA406946459MYH14c.283C>A (p.Gln95Lys)
c.-2008C>A (n.-2008C>A)
c.403C>A (p.Gln135Lys)
 gnomAD v4
19g.50210648C>GCA406946460MYH14c.283C>G (p.Gln95Glu)
c.-2008C>G (n.-2008C>G)
c.403C>G (p.Gln135Glu)
19g.50210648C>TCA406946462MYH14c.283C>T (p.Gln95Ter)
c.-2008C>T (n.-2008C>T)
c.403C>T (p.Gln135Ter)
 gnomAD v4
19g.50210649A>CCA406946469MYH14c.284A>C (p.Gln95Pro)
c.-2007A>C (n.-2007A>C)
c.404A>C (p.Gln135Pro)
19g.50210649A>GCA406946467MYH14c.284A>G (p.Gln95Arg)
c.-2007A>G (n.-2007A>G)
c.404A>G (p.Gln135Arg)
 gnomAD v4
19g.50210649A>TCA406946465MYH14c.284A>T (p.Gln95Leu)
c.-2007A>T (n.-2007A>T)
c.404A>T (p.Gln135Leu)
19g.50210650G>ACA508175229MYH14c.285G>A (p.Gln95=)
c.-2006G>A (n.-2006G>A)
c.405G>A (p.Gln135=)
19g.50210650G>CCA406946471MYH14c.285G>C (p.Gln95His)
c.-2006G>C (n.-2006G>C)
c.405G>C (p.Gln135His)
 ClinVar
19g.50210650G=CA2340790539MYH14c.285G= (p.Gln95=)
c.-2006G= (n.-2006G=)
c.405G= (p.Gln135=)
19g.50210650G>TCA406946472MYH14c.285G>T (p.Gln95His)
c.-2006G>T (n.-2006G>T)
c.405G>T (p.Gln135His)
 dbSNP gnomAD v2 gnomAD v4
19g.50210651A>CCA406946475MYH14c.286A>C (p.Ile96Leu)
c.-2005A>C (n.-2005A>C)
c.406A>C (p.Ile136Leu)
19g.50210651A>GCA406946477MYH14c.286A>G (p.Ile96Val)
c.-2005A>G (n.-2005A>G)
c.406A>G (p.Ile136Val)
 gnomAD v4
19g.50210651A>TCA406946478MYH14c.286A>T (p.Ile96Phe)
c.-2005A>T (n.-2005A>T)
c.406A>T (p.Ile136Phe)
 gnomAD v4
19g.50210652T>ACA406946481MYH14c.287T>A (p.Ile96Asn)
c.-2004T>A (n.-2004T>A)
c.407T>A (p.Ile136Asn)
19g.50210652T>CCA406946482MYH14c.287T>C (p.Ile96Thr)
c.-2004T>C (n.-2004T>C)
c.407T>C (p.Ile136Thr)
19g.50210652T>GCA406946483MYH14c.287T>G (p.Ile96Ser)
c.-2004T>G (n.-2004T>G)
c.407T>G (p.Ile136Ser)
19g.50210653C>ACA508175232MYH14c.288C>A (p.Ile96=)
c.-2003C>A (n.-2003C>A)
c.408C>A (p.Ile136=)
 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210653C=CA2340790540MYH14c.288C= (p.Ile96=)
c.-2003C= (n.-2003C=)
c.408C= (p.Ile136=)
19g.50210653C>GCA406946486MYH14c.288C>G (p.Ile96Met)
c.-2003C>G (n.-2003C>G)
c.408C>G (p.Ile136Met)
19g.50210653C>TCA508175231MYH14c.288C>T (p.Ile96=)
c.-2003C>T (n.-2003C>T)
c.408C>T (p.Ile136=)
 dbSNP gnomAD v2 gnomAD v4
19g.50210654C>ACA406946488MYH14c.289C>A (p.Gln97Lys)
c.-2002C>A (n.-2002C>A)
c.409C>A (p.Gln137Lys)
 gnomAD v4
19g.50210654C>GCA406946490MYH14c.289C>G (p.Gln97Glu)
c.-2002C>G (n.-2002C>G)
c.409C>G (p.Gln137Glu)
 gnomAD v4
19g.50210654C>TCA406946492MYH14c.289C>T (p.Gln97Ter)
c.-2002C>T (n.-2002C>T)
c.409C>T (p.Gln137Ter)
19g.50210654_50210655insTGGCA2695229032MYH14c.289_290insTGG (p.Gln97delinsLeuGlu)
c.-2002_-2001insTGG (n.-2002_-2001insTGG)
c.409_410insTGG (p.Gln137delinsLeuGlu)
19g.50210655A=CA2340790541MYH14c.290A= (p.Gln97=)
c.-2001A= (n.-2001A=)
c.410A= (p.Gln137=)
19g.50210655A>CCA406946497MYH14c.290A>C (p.Gln97Pro)
c.-2001A>C (n.-2001A>C)
c.410A>C (p.Gln137Pro)
19g.50210655A>GCA406946496MYH14c.290A>G (p.Gln97Arg)
c.-2001A>G (n.-2001A>G)
c.410A>G (p.Gln137Arg)
 dbSNP gnomAD v2 gnomAD v4
19g.50210655A>TCA406946494MYH14c.290A>T (p.Gln97Leu)
c.-2001A>T (n.-2001A>T)
c.410A>T (p.Gln137Leu)
19g.50210656G>ACA508175235MYH14c.291G>A (p.Gln97=)
c.-2000G>A (n.-2000G>A)
c.411G>A (p.Gln137=)
19g.50210656G>CCA406946499MYH14c.291G>C (p.Gln97His)
c.-2000G>C (n.-2000G>C)
c.411G>C (p.Gln137His)
19g.50210656G>TCA406946501MYH14c.291G>T (p.Gln97His)
c.-2000G>T (n.-2000G>T)
c.411G>T (p.Gln137His)
 gnomAD v4
19g.50210657C>ACA406946503MYH14c.292C>A (p.Arg98Ser)
c.-1999C>A (n.-1999C>A)
c.412C>A (p.Arg138Ser)
 dbSNP gnomAD v4
19g.50210657C=CA2340790542MYH14c.292C= (p.Arg98=)
c.-1999C= (n.-1999C=)
c.412C= (p.Arg138=)
19g.50210657C>GCA406946505MYH14c.292C>G (p.Arg98Gly)
c.-1999C>G (n.-1999C>G)
c.412C>G (p.Arg138Gly)
19g.50210657C>TCA406946506MYH14c.292C>T (p.Arg98Cys)
c.-1999C>T (n.-1999C>T)
c.412C>T (p.Arg138Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210658G>ACA309565626MYH14c.293G>A (p.Arg98His)
c.-1998G>A (n.-1998G>A)
c.413G>A (p.Arg138His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.50210658G>CCA9592222MYH14c.293G>C (p.Arg98Pro)
c.-1998G>C (n.-1998G>C)
c.413G>C (p.Arg138Pro)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210658G=CA2340790543MYH14c.293G= (p.Arg98=)
c.-1998G= (n.-1998G=)
c.413G= (p.Arg138=)
19g.50210658G>TCA406946510MYH14c.293G>T (p.Arg98Leu)
c.-1998G>T (n.-1998G>T)
c.413G>T (p.Arg138Leu)
 gnomAD v4
19g.50210659C>ACA508175239MYH14c.294C>A (p.Arg98=)
c.-1997C>A (n.-1997C>A)
c.414C>A (p.Arg138=)
19g.50210659C>GCA508175242MYH14c.294C>G (p.Arg98=)
c.-1997C>G (n.-1997C>G)
c.414C>G (p.Arg138=)
 gnomAD v4
19g.50210659C>TCA508175240MYH14c.294C>T (p.Arg98=)
c.-1997C>T (n.-1997C>T)
c.414C>T (p.Arg138=)
 gnomAD v4
19g.50210660A>CCA406946511MYH14c.295A>C (p.Met99Leu)
c.-1996A>C (n.-1996A>C)
c.415A>C (p.Met139Leu)
19g.50210660A>GCA406946512MYH14c.295A>G (p.Met99Val)
c.-1996A>G (n.-1996A>G)
c.415A>G (p.Met139Val)
19g.50210660A>TCA406946513MYH14c.295A>T (p.Met99Leu)
c.-1996A>T (n.-1996A>T)
c.415A>T (p.Met139Leu)
19g.50210661T>ACA406946514MYH14c.296T>A (p.Met99Lys)
c.-1995T>A (n.-1995T>A)
c.416T>A (p.Met139Lys)
19g.50210661T>CCA406946515MYH14c.296T>C (p.Met99Thr)
c.-1995T>C (n.-1995T>C)
c.416T>C (p.Met139Thr)
19g.50210661T>GCA406946516MYH14c.296T>G (p.Met99Arg)
c.-1995T>G (n.-1995T>G)
c.416T>G (p.Met139Arg)
19g.50210662G>ACA406946519MYH14c.297G>A (p.Met99Ile)
c.-1994G>A (n.-1994G>A)
c.417G>A (p.Met139Ile)
19g.50210662G>CCA406946517MYH14c.297G>C (p.Met99Ile)
c.-1994G>C (n.-1994G>C)
c.417G>C (p.Met139Ile)
19g.50210662G>TCA406946518MYH14c.297G>T (p.Met99Ile)
c.-1994G>T (n.-1994G>T)
c.417G>T (p.Met139Ile)
 gnomAD v4
19g.50210663A>CCA406946520MYH14c.298A>C (p.Asn100His)
c.-1993A>C (n.-1993A>C)
c.418A>C (p.Asn140His)
19g.50210663A>GCA406946521MYH14c.298A>G (p.Asn100Asp)
c.-1993A>G (n.-1993A>G)
c.418A>G (p.Asn140Asp)
19g.50210663A>TCA406946522MYH14c.298A>T (p.Asn100Tyr)
c.-1993A>T (n.-1993A>T)
c.418A>T (p.Asn140Tyr)
19g.50210664A=CA2340790544MYH14c.299A= (p.Asn100=)
c.-1992A= (n.-1992A=)
c.419A= (p.Asn140=)
19g.50210664A>CCA309565631MYH14c.299A>C (p.Asn100Thr)
c.-1992A>C (n.-1992A>C)
c.419A>C (p.Asn140Thr)
 dbSNP gnomAD v4 COSMIC COSMIC COSMIC
19g.50210664A>GCA406946523MYH14c.299A>G (p.Asn100Ser)
c.-1992A>G (n.-1992A>G)
c.419A>G (p.Asn140Ser)
 gnomAD v4
19g.50210664A>TCA406946524MYH14c.299A>T (p.Asn100Ile)
c.-1992A>T (n.-1992A>T)
c.419A>T (p.Asn140Ile)
19g.50210665C>ACA406946525MYH14c.300C>A (p.Asn100Lys)
c.-1991C>A (n.-1991C>A)
c.420C>A (p.Asn140Lys)
 gnomAD v4
19g.50210665C>GCA406946526MYH14c.300C>G (p.Asn100Lys)
c.-1991C>G (n.-1991C>G)
c.420C>G (p.Asn140Lys)
19g.50210665C>TCA508175246MYH14c.300C>T (p.Asn100=)
c.-1991C>T (n.-1991C>T)
c.420C>T (p.Asn140=)
 gnomAD v4
19g.50210666C>ACA406946527MYH14c.301C>A (p.Pro101Thr)
c.-1990C>A (n.-1990C>A)
c.421C>A (p.Pro141Thr)
19g.50210666C>GCA406946528MYH14c.301C>G (p.Pro101Ala)
c.-1990C>G (n.-1990C>G)
c.421C>G (p.Pro141Ala)
19g.50210666C>TCA406946529MYH14c.301C>T (p.Pro101Ser)
c.-1990C>T (n.-1990C>T)
c.421C>T (p.Pro141Ser)
19g.50210667C>ACA406946531MYH14c.302C>A (p.Pro101Gln)
c.-1989C>A (n.-1989C>A)
c.422C>A (p.Pro141Gln)
 gnomAD v4
19g.50210667C>GCA406946532MYH14c.302C>G (p.Pro101Arg)
c.-1989C>G (n.-1989C>G)
c.422C>G (p.Pro141Arg)
19g.50210667C>TCA406946530MYH14c.302C>T (p.Pro101Leu)
c.-1989C>T (n.-1989C>T)
c.422C>T (p.Pro141Leu)
 gnomAD v4
19g.50210668G>ACA9592223MYH14c.303G>A (p.Pro101=)
c.-1988G>A (n.-1988G>A)
c.423G>A (p.Pro141=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210668G>CCA309565636MYH14c.303G>C (p.Pro101=)
c.-1988G>C (n.-1988G>C)
c.423G>C (p.Pro141=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210668G=CA2340790545MYH14c.303G= (p.Pro101=)
c.-1988G= (n.-1988G=)
c.423G= (p.Pro141=)
19g.50210668G>TCA508175248MYH14c.303G>T (p.Pro101=)
c.-1988G>T (n.-1988G>T)
c.423G>T (p.Pro141=)
 gnomAD v4
19g.50210669C>ACA406946533MYH14c.304C>A (p.Pro102Thr)
c.-1987C>A (n.-1987C>A)
c.424C>A (p.Pro142Thr)
19g.50210669C=CA2340790546MYH14c.304C= (p.Pro102=)
c.-1987C= (n.-1987C=)
c.424C= (p.Pro142=)
19g.50210669C>GCA406946534MYH14c.304C>G (p.Pro102Ala)
c.-1987C>G (n.-1987C>G)
c.424C>G (p.Pro142Ala)
19g.50210669C>TCA406946535MYH14c.304C>T (p.Pro102Ser)
c.-1987C>T (n.-1987C>T)
c.424C>T (p.Pro142Ser)
 dbSNP gnomAD v2 gnomAD v4
19g.50210670C>ACA406946536MYH14c.305C>A (p.Pro102His)
c.-1986C>A (n.-1986C>A)
c.425C>A (p.Pro142His)
 gnomAD v4
19g.50210670C>GCA406946537MYH14c.305C>G (p.Pro102Arg)
c.-1986C>G (n.-1986C>G)
c.425C>G (p.Pro142Arg)
 gnomAD v4
19g.50210670C>TCA406946538MYH14c.305C>T (p.Pro102Leu)
c.-1986C>T (n.-1986C>T)
c.425C>T (p.Pro142Leu)
 gnomAD v4
19g.50210671C>ACA508175250MYH14c.306C>A (p.Pro102=)
c.-1985C>A (n.-1985C>A)
c.426C>A (p.Pro142=)
19g.50210671C=CA2340790547MYH14c.306C= (p.Pro102=)
c.-1985C= (n.-1985C=)
c.426C= (p.Pro142=)
19g.50210671C>GCA508175251MYH14c.306C>G (p.Pro102=)
c.-1985C>G (n.-1985C>G)
c.426C>G (p.Pro142=)
19g.50210671C>TCA508175253MYH14c.306C>T (p.Pro102=)
c.-1985C>T (n.-1985C>T)
c.426C>T (p.Pro142=)
 dbSNP gnomAD v3 gnomAD v4
19g.50210672A=CA2340790548MYH14c.307A= (p.Lys103=)
c.-1984A= (n.-1984A=)
c.427A= (p.Lys143=)
19g.50210672A>CCA406946539MYH14c.307A>C (p.Lys103Gln)
c.-1984A>C (n.-1984A>C)
c.427A>C (p.Lys143Gln)
19g.50210672A>GCA9592224MYH14c.307A>G (p.Lys103Glu)
c.-1984A>G (n.-1984A>G)
c.427A>G (p.Lys143Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210672A>TCA406946540MYH14c.307A>T (p.Lys103Ter)
c.-1984A>T (n.-1984A>T)
c.427A>T (p.Lys143Ter)
19g.50210673A=CA2340790549MYH14c.308A= (p.Lys103=)
c.-1983A= (n.-1983A=)
c.428A= (p.Lys143=)
19g.50210673A>CCA406946541MYH14c.308A>C (p.Lys103Thr)
c.-1983A>C (n.-1983A>C)
c.428A>C (p.Lys143Thr)
19g.50210673A>GCA309565645MYH14c.308A>G (p.Lys103Arg)
c.-1983A>G (n.-1983A>G)
c.428A>G (p.Lys143Arg)
 dbSNP gnomAD v2 gnomAD v4
19g.50210673A>TCA406946542MYH14c.308A>T (p.Lys103Met)
c.-1983A>T (n.-1983A>T)
c.428A>T (p.Lys143Met)
19g.50210674G>ACA508175255MYH14c.309G>A (p.Lys103=)
c.-1982G>A (n.-1982G>A)
c.429G>A (p.Lys143=)
19g.50210674G>CCA406946544MYH14c.309G>C (p.Lys103Asn)
c.-1982G>C (n.-1982G>C)
c.429G>C (p.Lys143Asn)
19g.50210674G>TCA406946543MYH14c.309G>T (p.Lys103Asn)
c.-1982G>T (n.-1982G>T)
c.429G>T (p.Lys143Asn)
 gnomAD v4
19g.50210675T>ACA406946545MYH14c.310T>A (p.Phe104Ile)
c.-1981T>A (n.-1981T>A)
c.430T>A (p.Phe144Ile)
 gnomAD v4
19g.50210675T>CCA406946546MYH14c.310T>C (p.Phe104Leu)
c.-1981T>C (n.-1981T>C)
c.430T>C (p.Phe144Leu)
 gnomAD v4
19g.50210675T>GCA406946547MYH14c.310T>G (p.Phe104Val)
c.-1981T>G (n.-1981T>G)
c.430T>G (p.Phe144Val)
19g.50210676T>ACA406946548MYH14c.311T>A (p.Phe104Tyr)
c.-1980T>A (n.-1980T>A)
c.431T>A (p.Phe144Tyr)
19g.50210676T>CCA406946549MYH14c.311T>C (p.Phe104Ser)
c.-1980T>C (n.-1980T>C)
c.431T>C (p.Phe144Ser)
19g.50210676T>GCA406946550MYH14c.311T>G (p.Phe104Cys)
c.-1980T>G (n.-1980T>G)
c.431T>G (p.Phe144Cys)
19g.50210677C>ACA406946551MYH14c.312C>A (p.Phe104Leu)
c.-1979C>A (n.-1979C>A)
c.432C>A (p.Phe144Leu)
 gnomAD v4
19g.50210677C=CA2340790550MYH14c.312C= (p.Phe104=)
c.-1979C= (n.-1979C=)
c.432C= (p.Phe144=)
19g.50210677C>GCA406946552MYH14c.312C>G (p.Phe104Leu)
c.-1979C>G (n.-1979C>G)
c.432C>G (p.Phe144Leu)
19g.50210677C>TCA508175256MYH14c.312C>T (p.Phe104=)
c.-1979C>T (n.-1979C>T)
c.432C>T (p.Phe144=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210678A=CA2340790551MYH14c.313A= (p.Ser105=)
c.-1978A= (n.-1978A=)
c.433A= (p.Ser145=)
19g.50210678A>CCA406946553MYH14c.313A>C (p.Ser105Arg)
c.-1978A>C (n.-1978A>C)
c.433A>C (p.Ser145Arg)
19g.50210678A>GCA406946554MYH14c.313A>G (p.Ser105Gly)
c.-1978A>G (n.-1978A>G)
c.433A>G (p.Ser145Gly)
 gnomAD v4
19g.50210678A>TCA406946555MYH14c.313A>T (p.Ser105Cys)
c.-1978A>T (n.-1978A>T)
c.433A>T (p.Ser145Cys)
 dbSNP gnomAD v2 gnomAD v4
19g.50210679G>ACA406946556MYH14c.314G>A (p.Ser105Asn)
c.-1977G>A (n.-1977G>A)
c.434G>A (p.Ser145Asn)
 gnomAD v4
19g.50210679G>CCA406946557MYH14c.314G>C (p.Ser105Thr)
c.-1977G>C (n.-1977G>C)
c.434G>C (p.Ser145Thr)
 dbSNP
19g.50210679G>TCA406946558MYH14c.314G>T (p.Ser105Ile)
c.-1977G>T (n.-1977G>T)
c.434G>T (p.Ser145Ile)
 gnomAD v4
19g.50210680C>ACA406946559MYH14c.315C>A (p.Ser105Arg)
c.-1976C>A (n.-1976C>A)
c.435C>A (p.Ser145Arg)
 gnomAD v4
19g.50210680C>GCA406946560MYH14c.315C>G (p.Ser105Arg)
c.-1976C>G (n.-1976C>G)
c.435C>G (p.Ser145Arg)
19g.50210680C>TCA508175257MYH14c.315C>T (p.Ser105=)
c.-1976C>T (n.-1976C>T)
c.435C>T (p.Ser145=)
 gnomAD v4
19g.50210681A>CCA406946561MYH14c.316A>C (p.Lys106Gln)
c.-1975A>C (n.-1975A>C)
c.436A>C (p.Lys146Gln)
 gnomAD v4
19g.50210681A>GCA406946563MYH14c.316A>G (p.Lys106Glu)
c.-1975A>G (n.-1975A>G)
c.436A>G (p.Lys146Glu)
19g.50210681A>TCA406946562MYH14c.316A>T (p.Lys106Ter)
c.-1975A>T (n.-1975A>T)
c.436A>T (p.Lys146Ter)
19g.50210682A>CCA406946564MYH14c.317A>C (p.Lys106Thr)
c.-1974A>C (n.-1974A>C)
c.437A>C (p.Lys146Thr)
19g.50210682A>GCA406946566MYH14c.317A>G (p.Lys106Arg)
c.-1974A>G (n.-1974A>G)
c.437A>G (p.Lys146Arg)
19g.50210682A>TCA406946565MYH14c.317A>T (p.Lys106Met)
c.-1974A>T (n.-1974A>T)
c.437A>T (p.Lys146Met)
19g.50210683G>ACA508175258MYH14c.318G>A (p.Lys106=)
c.-1973G>A (n.-1973G>A)
c.438G>A (p.Lys146=)
 gnomAD v4
19g.50210683G>CCA406946567MYH14c.318G>C (p.Lys106Asn)
c.-1973G>C (n.-1973G>C)
c.438G>C (p.Lys146Asn)
 gnomAD v4
19g.50210683G>TCA406946568MYH14c.318G>T (p.Lys106Asn)
c.-1973G>T (n.-1973G>T)
c.438G>T (p.Lys146Asn)
 gnomAD v4
19g.50210684G>ACA406946569MYH14c.319G>A (p.Ala107Thr)
c.-1972G>A (n.-1972G>A)
c.439G>A (p.Ala147Thr)
 gnomAD v4
19g.50210684G>CCA406946570MYH14c.319G>C (p.Ala107Pro)
c.-1972G>C (n.-1972G>C)
c.439G>C (p.Ala147Pro)
19g.50210684G>TCA406946571MYH14c.319G>T (p.Ala107Ser)
c.-1972G>T (n.-1972G>T)
c.439G>T (p.Ala147Ser)
 gnomAD v4
19g.50210685C>ACA406946572MYH14c.320C>A (p.Ala107Asp)
c.-1971C>A (n.-1971C>A)
c.440C>A (p.Ala147Asp)
19g.50210685C=CA2340790552MYH14c.320C= (p.Ala107=)
c.-1971C= (n.-1971C=)
c.440C= (p.Ala147=)
19g.50210685C>GCA406946573MYH14c.320C>G (p.Ala107Gly)
c.-1971C>G (n.-1971C>G)
c.440C>G (p.Ala147Gly)
19g.50210685C>TCA406946574MYH14c.320C>T (p.Ala107Val)
c.-1971C>T (n.-1971C>T)
c.440C>T (p.Ala147Val)
 dbSNP gnomAD v4
19g.50210686C>ACA508175259MYH14c.321C>A (p.Ala107=)
c.-1970C>A (n.-1970C>A)
c.441C>A (p.Ala147=)
 ClinVar dbSNP gnomAD v4
19g.50210686C=CA2340790553MYH14c.321C= (p.Ala107=)
c.-1970C= (n.-1970C=)
c.441C= (p.Ala147=)
19g.50210686C>GCA508175260MYH14c.321C>G (p.Ala107=)
c.-1970C>G (n.-1970C>G)
c.441C>G (p.Ala147=)
 gnomAD v4
19g.50210686C>TCA508175261MYH14c.321C>T (p.Ala107=)
c.-1970C>T (n.-1970C>T)
c.441C>T (p.Ala147=)
 dbSNP gnomAD v4
19g.50210687G>ACA9592225MYH14c.322G>A (p.Glu108Lys)
c.-1969G>A (n.-1969G>A)
c.442G>A (p.Glu148Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210687G>CCA406946575MYH14c.322G>C (p.Glu108Gln)
c.-1969G>C (n.-1969G>C)
c.442G>C (p.Glu148Gln)
 dbSNP gnomAD v4
19g.50210687G=CA2340790554MYH14c.322G= (p.Glu108=)
c.-1969G= (n.-1969G=)
c.442G= (p.Glu148=)
19g.50210687G>TCA406946576MYH14c.322G>T (p.Glu108Ter)
c.-1969G>T (n.-1969G>T)
c.442G>T (p.Glu148Ter)
 gnomAD v4
19g.50210688A>CCA406946577MYH14c.323A>C (p.Glu108Ala)
c.-1968A>C (n.-1968A>C)
c.443A>C (p.Glu148Ala)
19g.50210688A>GCA406946578MYH14c.323A>G (p.Glu108Gly)
c.-1968A>G (n.-1968A>G)
c.443A>G (p.Glu148Gly)
 gnomAD v4
19g.50210688A>TCA406946579MYH14c.323A>T (p.Glu108Val)
c.-1968A>T (n.-1968A>T)
c.443A>T (p.Glu148Val)
19g.50210689G>ACA309565660MYH14c.324G>A (p.Glu108=)
c.-1967G>A (n.-1967G>A)
c.444G>A (p.Glu148=)
 dbSNP gnomAD v4
19g.50210689G>CCA406946580MYH14c.324G>C (p.Glu108Asp)
c.-1967G>C (n.-1967G>C)
c.444G>C (p.Glu148Asp)
19g.50210689G=CA2340790555MYH14c.324G= (p.Glu108=)
c.-1967G= (n.-1967G=)
c.444G= (p.Glu148=)
19g.50210689G>TCA406946581MYH14c.324G>T (p.Glu108Asp)
c.-1967G>T (n.-1967G>T)
c.444G>T (p.Glu148Asp)
 gnomAD v4
19g.50210690G>ACA406946582MYH14c.325G>A (p.Asp109Asn)
c.-1966G>A (n.-1966G>A)
c.445G>A (p.Asp149Asn)
19g.50210690G>CCA406946583MYH14c.325G>C (p.Asp109His)
c.-1966G>C (n.-1966G>C)
c.445G>C (p.Asp149His)
19g.50210690G>TCA406946584MYH14c.325G>T (p.Asp109Tyr)
c.-1966G>T (n.-1966G>T)
c.445G>T (p.Asp149Tyr)
19g.50210691A=CA2340790556MYH14c.326A= (p.Asp109=)
c.-1965A= (n.-1965A=)
c.446A= (p.Asp149=)
19g.50210691A>CCA406946585MYH14c.326A>C (p.Asp109Ala)
c.-1965A>C (n.-1965A>C)
c.446A>C (p.Asp149Ala)
 dbSNP gnomAD v2 gnomAD v4
19g.50210691A>GCA406946586MYH14c.326A>G (p.Asp109Gly)
c.-1965A>G (n.-1965A>G)
c.446A>G (p.Asp149Gly)
19g.50210691A>TCA406946587MYH14c.326A>T (p.Asp109Val)
c.-1965A>T (n.-1965A>T)
c.446A>T (p.Asp149Val)
19g.50210692C>ACA406946588MYH14c.327C>A (p.Asp109Glu)
c.-1964C>A (n.-1964C>A)
c.447C>A (p.Asp149Glu)
19g.50210692C=CA2340790557MYH14c.327C= (p.Asp109=)
c.-1964C= (n.-1964C=)
c.447C= (p.Asp149=)
19g.50210692C>GCA406946589MYH14c.327C>G (p.Asp109Glu)
c.-1964C>G (n.-1964C>G)
c.447C>G (p.Asp149Glu)
19g.50210692C>TCA9592226MYH14c.327C>T (p.Asp109=)
c.-1964C>T (n.-1964C>T)
c.447C>T (p.Asp149=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.50210693A=CA2340790558MYH14c.328A= (p.Met110=)
c.-1963A= (n.-1963A=)
c.448A= (p.Met150=)
19g.50210693A>CCA406946590MYH14c.328A>C (p.Met110Leu)
c.-1963A>C (n.-1963A>C)
c.448A>C (p.Met150Leu)
19g.50210693A>GCA406946591MYH14c.328A>G (p.Met110Val)
c.-1963A>G (n.-1963A>G)
c.448A>G (p.Met150Val)
 dbSNP gnomAD v4
19g.50210693A>TCA406946592MYH14c.328A>T (p.Met110Leu)
c.-1963A>T (n.-1963A>T)
c.448A>T (p.Met150Leu)
 dbSNP
19g.50210694T>ACA406946593MYH14c.329T>A (p.Met110Lys)
c.-1962T>A (n.-1962T>A)
c.449T>A (p.Met150Lys)
19g.50210694T>CCA406946595MYH14c.329T>C (p.Met110Thr)
c.-1962T>C (n.-1962T>C)
c.449T>C (p.Met150Thr)
 gnomAD v4
19g.50210694T>GCA406946594MYH14c.329T>G (p.Met110Arg)
c.-1962T>G (n.-1962T>G)
c.449T>G (p.Met150Arg)
19g.50210695G>ACA406946596MYH14c.330G>A (p.Met110Ile)
c.-1961G>A (n.-1961G>A)
c.450G>A (p.Met150Ile)
19g.50210695G>CCA406946597MYH14c.330G>C (p.Met110Ile)
c.-1961G>C (n.-1961G>C)
c.450G>C (p.Met150Ile)
19g.50210695G>TCA406946598MYH14c.330G>T (p.Met110Ile)
c.-1961G>T (n.-1961G>T)
c.450G>T (p.Met150Ile)
 gnomAD v4
19g.50210696G>ACA406946599MYH14c.331G>A (p.Ala111Thr)
c.-1960G>A (n.-1960G>A)
c.451G>A (p.Ala151Thr)
 gnomAD v4
19g.50210696G>CCA406946600MYH14c.331G>C (p.Ala111Pro)
c.-1960G>C (n.-1960G>C)
c.451G>C (p.Ala151Pro)
19g.50210696G>TCA406946601MYH14c.331G>T (p.Ala111Ser)
c.-1960G>T (n.-1960G>T)
c.451G>T (p.Ala151Ser)
 gnomAD v4
19g.50210697C>ACA406946602MYH14c.332C>A (p.Ala111Asp)
c.-1959C>A (n.-1959C>A)
c.452C>A (p.Ala151Asp)
19g.50210697C>GCA406946603MYH14c.332C>G (p.Ala111Gly)
c.-1959C>G (n.-1959C>G)
c.452C>G (p.Ala151Gly)
19g.50210697C>TCA406946604MYH14c.332C>T (p.Ala111Val)
c.-1959C>T (n.-1959C>T)
c.452C>T (p.Ala151Val)
 gnomAD v4
19g.50210698C>ACA508175263MYH14c.333C>A (p.Ala111=)
c.-1958C>A (n.-1958C>A)
c.453C>A (p.Ala151=)
 gnomAD v4
19g.50210698C=CA2340790559MYH14c.333C= (p.Ala111=)
c.-1958C= (n.-1958C=)
c.453C= (p.Ala151=)
19g.50210698C>GCA508175262MYH14c.333C>G (p.Ala111=)
c.-1958C>G (n.-1958C>G)
c.453C>G (p.Ala151=)
 gnomAD v4
19g.50210698C>TCA309565673MYH14c.333C>T (p.Ala111=)
c.-1958C>T (n.-1958C>T)
c.453C>T (p.Ala151=)
 ClinVar dbSNP gnomAD v4
19g.50210699G>ACA406946605MYH14c.334G>A (p.Glu112Lys)
c.-1957G>A (n.-1957G>A)
c.454G>A (p.Glu152Lys)
 gnomAD v4
19g.50210699G>CCA406946606MYH14c.334G>C (p.Glu112Gln)
c.-1957G>C (n.-1957G>C)
c.454G>C (p.Glu152Gln)
 gnomAD v4
19g.50210699G>TCA406946607MYH14c.334G>T (p.Glu112Ter)
c.-1957G>T (n.-1957G>T)
c.454G>T (p.Glu152Ter)
 gnomAD v4
19g.50210700A>CCA406946608MYH14c.335A>C (p.Glu112Ala)
c.-1956A>C (n.-1956A>C)
c.455A>C (p.Glu152Ala)
19g.50210700A>GCA406946610MYH14c.335A>G (p.Glu112Gly)
c.-1956A>G (n.-1956A>G)
c.455A>G (p.Glu152Gly)
19g.50210700A>TCA406946609MYH14c.335A>T (p.Glu112Val)
c.-1956A>T (n.-1956A>T)
c.455A>T (p.Glu152Val)
19g.50210701G>ACA508175264MYH14c.336G>A (p.Glu112=)
c.-1955G>A (n.-1955G>A)
c.456G>A (p.Glu152=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210701G>CCA406946611MYH14c.336G>C (p.Glu112Asp)
c.-1955G>C (n.-1955G>C)
c.456G>C (p.Glu152Asp)
19g.50210701G=CA2340790560MYH14c.336G= (p.Glu112=)
c.-1955G= (n.-1955G=)
c.456G= (p.Glu152=)
19g.50210701G>TCA406946612MYH14c.336G>T (p.Glu112Asp)
c.-1955G>T (n.-1955G>T)
c.456G>T (p.Glu152Asp)
 gnomAD v4
19g.50210702C>ACA406946613MYH14c.337C>A (p.Leu113Met)
c.-1954C>A (n.-1954C>A)
c.457C>A (p.Leu153Met)
19g.50210702C>GCA406946614MYH14c.337C>G (p.Leu113Val)
c.-1954C>G (n.-1954C>G)
c.457C>G (p.Leu153Val)
 gnomAD v4
19g.50210702C>TCA508175265MYH14c.337C>T (p.Leu113=)
c.-1954C>T (n.-1954C>T)
c.457C>T (p.Leu153=)
19g.50210703T>ACA406946615MYH14c.338T>A (p.Leu113Gln)
c.-1953T>A (n.-1953T>A)
c.458T>A (p.Leu153Gln)
19g.50210703T>CCA309565675MYH14c.338T>C (p.Leu113Pro)
c.-1953T>C (n.-1953T>C)
c.458T>C (p.Leu153Pro)
 dbSNP gnomAD v4
19g.50210703T>GCA406946616MYH14c.338T>G (p.Leu113Arg)
c.-1953T>G (n.-1953T>G)
c.458T>G (p.Leu153Arg)
19g.50210703T=CA2340790561MYH14c.338T= (p.Leu113=)
c.-1953T= (n.-1953T=)
c.458T= (p.Leu153=)
19g.50210704G>ACA508175266MYH14c.339G>A (p.Leu113=)
c.-1952G>A (n.-1952G>A)
c.459G>A (p.Leu153=)
 gnomAD v4
19g.50210704G>CCA508175267MYH14c.339G>C (p.Leu113=)
c.-1952G>C (n.-1952G>C)
c.459G>C (p.Leu153=)
19g.50210704G>TCA508175268MYH14c.339G>T (p.Leu113=)
c.-1952G>T (n.-1952G>T)
c.459G>T (p.Leu153=)
 gnomAD v4
19g.50210705A=CA2340790052MYH14c.340A= (p.Thr114=)
c.-1951A= (n.-1951A=)
c.460A= (p.Thr154=)
19g.50210705A>CCA9592227MYH14c.340A>C (p.Thr114Pro)
c.-1951A>C (n.-1951A>C)
c.460A>C (p.Thr154Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.50210705A>GCA406946617MYH14c.340A>G (p.Thr114Ala)
c.-1951A>G (n.-1951A>G)
c.460A>G (p.Thr154Ala)
 gnomAD v4
19g.50210705A>TCA406946618MYH14c.340A>T (p.Thr114Ser)
c.-1951A>T (n.-1951A>T)
c.460A>T (p.Thr154Ser)
19g.50210706C>ACA406946620MYH14c.341C>A (p.Thr114Asn)
c.-1950C>A (n.-1950C>A)
c.461C>A (p.Thr154Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.50210706C=CA2340790055MYH14c.341C= (p.Thr114=)
c.-1950C= (n.-1950C=)
c.461C= (p.Thr154=)
19g.50210706C>GCA406946621MYH14c.341C>G (p.Thr114Ser)
c.-1950C>G (n.-1950C>G)
c.461C>G (p.Thr154Ser)
19g.50210706C>TCA406946619MYH14c.341C>T (p.Thr114Ile)
c.-1950C>T (n.-1950C>T)
c.461C>T (p.Thr154Ile)
 gnomAD v4
19g.50210707C>ACA508175269MYH14c.342C>A (p.Thr114=)
c.-1949C>A (n.-1949C>A)
c.462C>A (p.Thr154=)
 gnomAD v4
19g.50210707C>GCA508175270MYH14c.342C>G (p.Thr114=)
c.-1949C>G (n.-1949C>G)
c.462C>G (p.Thr154=)
19g.50210707C>TCA508175271MYH14c.342C>T (p.Thr114=)
c.-1949C>T (n.-1949C>T)
c.462C>T (p.Thr154=)
 gnomAD v4
19g.50210708T>ACA406946624MYH14c.343T>A (p.Cys115Ser)
c.-1948T>A (n.-1948T>A)
c.463T>A (p.Cys155Ser)
19g.50210708T>CCA406946622MYH14c.343T>C (p.Cys115Arg)
c.-1948T>C (n.-1948T>C)
c.463T>C (p.Cys155Arg)
19g.50210708T>GCA406946623MYH14c.343T>G (p.Cys115Gly)
c.-1948T>G (n.-1948T>G)
c.463T>G (p.Cys155Gly)
19g.50210709G>ACA406946625MYH14c.344G>A (p.Cys115Tyr)
c.-1947G>A (n.-1947G>A)
c.464G>A (p.Cys155Tyr)
19g.50210709G>CCA406946626MYH14c.344G>C (p.Cys115Ser)
c.-1947G>C (n.-1947G>C)
c.464G>C (p.Cys155Ser)
19g.50210709G>TCA406946627MYH14c.344G>T (p.Cys115Phe)
c.-1947G>T (n.-1947G>T)
c.464G>T (p.Cys155Phe)
 gnomAD v4
19g.50210710C>ACA406946628MYH14c.345C>A (p.Cys115Ter)
c.-1946C>A (n.-1946C>A)
c.465C>A (p.Cys155Ter)
 gnomAD v4
19g.50210710C>GCA406946629MYH14c.345C>G (p.Cys115Trp)
c.-1946C>G (n.-1946C>G)
c.465C>G (p.Cys155Trp)
19g.50210710C>TCA508175272MYH14c.345C>T (p.Cys115=)
c.-1946C>T (n.-1946C>T)
c.465C>T (p.Cys155=)
 gnomAD v4
19g.50210711C>ACA406946630MYH14c.346C>A (p.Leu116Ile)
c.-1945C>A (n.-1945C>A)
c.466C>A (p.Leu156Ile)
 gnomAD v4
19g.50210711C>GCA406946631MYH14c.346C>G (p.Leu116Val)
c.-1945C>G (n.-1945C>G)
c.466C>G (p.Leu156Val)
19g.50210711C>TCA406946632MYH14c.346C>T (p.Leu116Phe)
c.-1945C>T (n.-1945C>T)
c.466C>T (p.Leu156Phe)
19g.50210712T>ACA406946633MYH14c.347T>A (p.Leu116His)
c.-1944T>A (n.-1944T>A)
c.467T>A (p.Leu156His)
19g.50210712T>CCA406946634MYH14c.347T>C (p.Leu116Pro)
c.-1944T>C (n.-1944T>C)
c.467T>C (p.Leu156Pro)
19g.50210712T>GCA406946635MYH14c.347T>G (p.Leu116Arg)
c.-1944T>G (n.-1944T>G)
c.467T>G (p.Leu156Arg)
19g.50210713C>ACA508175273MYH14c.348C>A (p.Leu116=)
c.-1943C>A (n.-1943C>A)
c.468C>A (p.Leu156=)
 gnomAD v4
19g.50210713C>GCA508175274MYH14c.348C>G (p.Leu116=)
c.-1943C>G (n.-1943C>G)
c.468C>G (p.Leu156=)
19g.50210713C>TCA508175275MYH14c.348C>T (p.Leu116=)
c.-1943C>T (n.-1943C>T)
c.468C>T (p.Leu156=)
 gnomAD v4
19g.50210714A>CCA406946638MYH14c.349A>C (p.Asn117His)
c.-1942A>C (n.-1942A>C)
c.469A>C (p.Asn157His)
19g.50210714A>GCA406946636MYH14c.349A>G (p.Asn117Asp)
c.-1942A>G (n.-1942A>G)
c.469A>G (p.Asn157Asp)
 gnomAD v4
19g.50210714A>TCA406946637MYH14c.349A>T (p.Asn117Tyr)
c.-1942A>T (n.-1942A>T)
c.469A>T (p.Asn157Tyr)
19g.50210715A=CA2340790056MYH14c.350A= (p.Asn117=)
c.-1941A= (n.-1941A=)
c.470A= (p.Asn157=)
19g.50210715A>CCA406946639MYH14c.350A>C (p.Asn117Thr)
c.-1941A>C (n.-1941A>C)
c.470A>C (p.Asn157Thr)
19g.50210715A>GCA406946640MYH14c.350A>G (p.Asn117Ser)
c.-1941A>G (n.-1941A>G)
c.470A>G (p.Asn157Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210715A>TCA406946641MYH14c.350A>T (p.Asn117Ile)
c.-1941A>T (n.-1941A>T)
c.470A>T (p.Asn157Ile)
19g.50210716C>ACA406946643MYH14c.351C>A (p.Asn117Lys)
c.-1940C>A (n.-1940C>A)
c.471C>A (p.Asn157Lys)
 gnomAD v4
19g.50210716C=CA2340790057MYH14c.351C= (p.Asn117=)
c.-1940C= (n.-1940C=)
c.471C= (p.Asn157=)
19g.50210716C>GCA406946645MYH14c.351C>G (p.Asn117Lys)
c.-1940C>G (n.-1940C>G)
c.471C>G (p.Asn157Lys)
19g.50210716C>TCA9592228MYH14c.351C>T (p.Asn117=)
c.-1940C>T (n.-1940C>T)
c.471C>T (p.Asn157=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
19g.50210717G>ACA406946649MYH14c.352G>A (p.Glu118Lys)
c.-1939G>A (n.-1939G>A)
c.472G>A (p.Glu158Lys)
 gnomAD v4
19g.50210717G>CCA406946651MYH14c.352G>C (p.Glu118Gln)
c.-1939G>C (n.-1939G>C)
c.472G>C (p.Glu158Gln)
 dbSNP
19g.50210717G=CA2340790059MYH14c.352G= (p.Glu118=)
c.-1939G= (n.-1939G=)
c.472G= (p.Glu158=)
19g.50210717G>TCA406946652MYH14c.352G>T (p.Glu118Ter)
c.-1939G>T (n.-1939G>T)
c.472G>T (p.Glu158Ter)
 gnomAD v4
19g.50210718A>CCA406946655MYH14c.353A>C (p.Glu118Ala)
c.-1938A>C (n.-1938A>C)
c.473A>C (p.Glu158Ala)
19g.50210718A>GCA406946656MYH14c.353A>G (p.Glu118Gly)
c.-1938A>G (n.-1938A>G)
c.473A>G (p.Glu158Gly)
 gnomAD v4
19g.50210718A>TCA406946657MYH14c.353A>T (p.Glu118Val)
c.-1938A>T (n.-1938A>T)
c.473A>T (p.Glu158Val)
19g.50210719G>ACA508175276MYH14c.354G>A (p.Glu118=)
c.-1937G>A (n.-1937G>A)
c.474G>A (p.Glu158=)
 gnomAD v4
19g.50210719G>CCA406946660MYH14c.354G>C (p.Glu118Asp)
c.-1937G>C (n.-1937G>C)
c.474G>C (p.Glu158Asp)
 gnomAD v4
19g.50210719G>TCA406946662MYH14c.354G>T (p.Glu118Asp)
c.-1937G>T (n.-1937G>T)
c.474G>T (p.Glu158Asp)
 gnomAD v4
19g.50210720G>ACA406946663MYH14c.355G>A (p.Ala119Thr)
c.-1936G>A (n.-1936G>A)
c.475G>A (p.Ala159Thr)
 gnomAD v4
19g.50210720G>CCA406946665MYH14c.355G>C (p.Ala119Pro)
c.-1936G>C (n.-1936G>C)
c.475G>C (p.Ala159Pro)
19g.50210720G=CA2340790061MYH14c.355G= (p.Ala119=)
c.-1936G= (n.-1936G=)
c.475G= (p.Ala159=)
19g.50210720G>TCA406946667MYH14c.355G>T (p.Ala119Ser)
c.-1936G>T (n.-1936G>T)
c.475G>T (p.Ala159Ser)
 gnomAD v4
19g.50210721C>ACA406946669MYH14c.356C>A (p.Ala119Asp)
c.-1935C>A (n.-1935C>A)
c.476C>A (p.Ala159Asp)
 gnomAD v4
19g.50210721C=CA2340790064MYH14c.356C= (p.Ala119=)
c.-1935C= (n.-1935C=)
c.476C= (p.Ala159=)
19g.50210721C>GCA406946670MYH14c.356C>G (p.Ala119Gly)
c.-1935C>G (n.-1935C>G)
c.476C>G (p.Ala159Gly)
19g.50210721C>TCA406946672MYH14c.356C>T (p.Ala119Val)
c.-1935C>T (n.-1935C>T)
c.476C>T (p.Ala159Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.50210722dupCA309565686MYH14c.357dup (p.Ser120LeufsTer?)
c.-1934dup (n.-1934dup)
c.477dup (p.Ser160LeufsTer?)
 dbSNP
19g.50210722C>ACA508175277MYH14c.357C>A (p.Ala119=)
c.-1934C>A (n.-1934C>A)
c.477C>A (p.Ala159=)
 gnomAD v4
19g.50210722C>GCA508175278MYH14c.357C>G (p.Ala119=)
c.-1934C>G (n.-1934C>G)
c.477C>G (p.Ala159=)
19g.50210722C>TCA508175279MYH14c.357C>T (p.Ala119=)
c.-1934C>T (n.-1934C>T)
c.477C>T (p.Ala159=)
19g.50210723T>ACA406946675MYH14c.358T>A (p.Ser120Thr)
c.-1933T>A (n.-1933T>A)
c.478T>A (p.Ser160Thr)
 dbSNP gnomAD v4
19g.50210723T>CCA406946676MYH14c.358T>C (p.Ser120Pro)
c.-1933T>C (n.-1933T>C)
c.478T>C (p.Ser160Pro)
 gnomAD v4
19g.50210723T>GCA406946678MYH14c.358T>G (p.Ser120Ala)
c.-1933T>G (n.-1933T>G)
c.478T>G (p.Ser160Ala)
19g.50210724C>ACA406946681MYH14c.359C>A (p.Ser120Ter)
c.-1932C>A (n.-1932C>A)
c.479C>A (p.Ser160Ter)
 gnomAD v4
19g.50210724C=CA2340790068MYH14c.359C= (p.Ser120=)
c.-1932C= (n.-1932C=)
c.479C= (p.Ser160=)
19g.50210724C>GCA406946682MYH14c.359C>G (p.Ser120Trp)
c.-1932C>G (n.-1932C>G)
c.479C>G (p.Ser160Trp)
 gnomAD v4
19g.50210724C>TCA252137MYH14c.359C>T (p.Ser120Leu)
c.-1932C>T (n.-1932C>T)
c.479C>T (p.Ser160Leu)
 ClinVar dbSNP gnomAD v4
19g.50210725G>ACA508175280MYH14c.360G>A (p.Ser120=)
c.-1931G>A (n.-1931G>A)
c.480G>A (p.Ser160=)
 dbSNP gnomAD v4
19g.50210725G>CCA508175281MYH14c.360G>C (p.Ser120=)
c.-1931G>C (n.-1931G>C)
c.480G>C (p.Ser160=)
 gnomAD v4
19g.50210725G=CA2340790070MYH14c.360G= (p.Ser120=)
c.-1931G= (n.-1931G=)
c.480G= (p.Ser160=)
19g.50210725G>TCA508175282MYH14c.360G>T (p.Ser120=)
c.-1931G>T (n.-1931G>T)
c.480G>T (p.Ser160=)
 gnomAD v4
19g.50210726delCA2586537518MYH14c.361del (p.Val121SerfsTer?)
c.-1930del (n.-1930del)
c.481del (p.Val161SerfsTer?)
 gnomAD v4
19g.50210726G>ACA406946687MYH14c.361G>A (p.Val121Ile)
c.-1930G>A (n.-1930G>A)
c.481G>A (p.Val161Ile)
 gnomAD v4
19g.50210726G>CCA406946689MYH14c.361G>C (p.Val121Leu)
c.-1930G>C (n.-1930G>C)
c.481G>C (p.Val161Leu)
19g.50210726G>TCA406946685MYH14c.361G>T (p.Val121Phe)
c.-1930G>T (n.-1930G>T)
c.481G>T (p.Val161Phe)
19g.50210727T>ACA406946691MYH14c.362T>A (p.Val121Asp)
c.-1929T>A (n.-1929T>A)
c.482T>A (p.Val161Asp)
19g.50210727T>CCA406946693MYH14c.362T>C (p.Val121Ala)
c.-1929T>C (n.-1929T>C)
c.482T>C (p.Val161Ala)
19g.50210727T>GCA406946696MYH14c.362T>G (p.Val121Gly)
c.-1929T>G (n.-1929T>G)
c.482T>G (p.Val161Gly)
19g.50210728C>ACA508175283MYH14c.363C>A (p.Val121=)
c.-1928C>A (n.-1928C>A)
c.483C>A (p.Val161=)
 gnomAD v4 COSMIC COSMIC COSMIC
19g.50210728C>GCA508175284MYH14c.363C>G (p.Val121=)
c.-1928C>G (n.-1928C>G)
c.483C>G (p.Val161=)
 gnomAD v4
19g.50210728C>TCA508175285MYH14c.363C>T (p.Val121=)
c.-1928C>T (n.-1928C>T)
c.483C>T (p.Val161=)
 gnomAD v4
19g.50210729C>ACA406946697MYH14c.364C>A (p.Leu122Met)
c.-1927C>A (n.-1927C>A)
c.484C>A (p.Leu162Met)
 gnomAD v4
19g.50210729C>GCA406946699MYH14c.364C>G (p.Leu122Val)
c.-1927C>G (n.-1927C>G)
c.484C>G (p.Leu162Val)
19g.50210729C>TCA508175286MYH14c.364C>T (p.Leu122=)
c.-1927C>T (n.-1927C>T)
c.484C>T (p.Leu162=)
 gnomAD v4
19g.50210730T>ACA406946706MYH14c.365T>A (p.Leu122Gln)
c.-1926T>A (n.-1926T>A)
c.485T>A (p.Leu162Gln)
 gnomAD v4
19g.50210730T>CCA406946702MYH14c.365T>C (p.Leu122Pro)
c.-1926T>C (n.-1926T>C)
c.485T>C (p.Leu162Pro)
 dbSNP gnomAD v4
19g.50210730T>GCA406946704MYH14c.365T>G (p.Leu122Arg)
c.-1926T>G (n.-1926T>G)
c.485T>G (p.Leu162Arg)
19g.50210731G>ACA508175287MYH14c.366G>A (p.Leu122=)
c.-1925G>A (n.-1925G>A)
c.486G>A (p.Leu162=)
 gnomAD v4
19g.50210731G>CCA508175288MYH14c.366G>C (p.Leu122=)
c.-1925G>C (n.-1925G>C)
c.486G>C (p.Leu162=)
19g.50210731G>TCA508175289MYH14c.366G>T (p.Leu122=)
c.-1925G>T (n.-1925G>T)
c.486G>T (p.Leu162=)
 gnomAD v4

Number of alleles fetched