Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23396241C=CA2123417714MYH6c.2429+43G= (n.2429+43G=)
14g.23396241C>GCA7115467MYH6c.2429+43G>C (n.2429+43G>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396241C>TCA2624246035MYH6c.2429+43G>A (n.2429+43G>A)
gnomAD v4
14g.23396242T>GCA704273077MYH6c.2429+42A>C (n.2429+42A>C)
dbSNP gnomAD v3 gnomAD v4
14g.23396242T=CA2123417716MYH6c.2429+42A= (n.2429+42A=)
14g.23396243C>GCA2624246036MYH6c.2429+41G>C (n.2429+41G>C)
gnomAD v4
14g.23396244T>CCA612933783MYH6c.2429+40A>G (n.2429+40A>G)
dbSNP gnomAD v2 gnomAD v4
14g.23396244T=CA2123417718MYH6c.2429+40A= (n.2429+40A=)
14g.23396245A=CA2123417720MYH6c.2429+39T= (n.2429+39T=)
14g.23396245A>GCA7115468MYH6c.2429+39T>C (n.2429+39T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396246C=CA2123417722MYH6c.2429+38G= (n.2429+38G=)
14g.23396246C>GCA257789065MYH6c.2429+38G>C (n.2429+38G>C)
dbSNP
14g.23396246C>TCA704273080MYH6c.2429+38G>A (n.2429+38G>A)
dbSNP gnomAD v4
14g.23396247A=CA2123417724MYH6c.2429+37T= (n.2429+37T=)
14g.23396247A>GCA961064098MYH6c.2429+37T>C (n.2429+37T>C)
dbSNP gnomAD v3 gnomAD v4
14g.23396248T>ACA2624246046MYH6c.2429+36A>T (n.2429+36A>T)
gnomAD v4
14g.23396248T>CCA2537416173MYH6c.2429+36A>G (n.2429+36A>G)
14g.23396250T>GCA2624246047MYH6c.2429+34A>C (n.2429+34A>C)
gnomAD v4
14g.23396251C=CA2123417727MYH6c.2429+33G= (n.2429+33G=)
14g.23396251C>TCA612933786MYH6c.2429+33G>A (n.2429+33G>A)
dbSNP gnomAD v2 gnomAD v4
14g.23396253A>GCA2800874784MYH6c.2429+31T>C (n.2429+31T>C)
14g.23396254G>ACA257789076MYH6c.2429+30C>T (n.2429+30C>T)
dbSNP gnomAD v2 gnomAD v4
14g.23396254G>CCA612933787MYH6c.2429+30C>G (n.2429+30C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396254G=CA2123417733MYH6c.2429+30C= (n.2429+30C=)
14g.23396255T>ACA2624246058MYH6c.2429+29A>T (n.2429+29A>T)
gnomAD v4
14g.23396255T>CCA2123417738MYH6c.2429+29A>G (n.2429+29A>G)
dbSNP
14g.23396255T=CA2123417736MYH6c.2429+29A= (n.2429+29A=)
14g.23396260G>ACA2575486233MYH6c.2429+24C>T (n.2429+24C>T)
14g.23396260G>TCA2729046488MYH6c.2429+24C>A (n.2429+24C>A)
dbSNP
14g.23396261C>ACA2123417742MYH6c.2429+23G>T (n.2429+23G>T)
dbSNP
14g.23396261C=CA2123417741MYH6c.2429+23G= (n.2429+23G=)
14g.23396262C=CA2123417743MYH6c.2429+22G= (n.2429+22G=)
14g.23396262C>TCA612933791MYH6c.2429+22G>A (n.2429+22G>A)
dbSNP gnomAD v2 gnomAD v4
14g.23396263T>ACA7115469MYH6c.2429+21A>T (n.2429+21A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396263T=CA2123417747MYH6c.2429+21A= (n.2429+21A=)
14g.23396264C>TCA2624246072MYH6c.2429+20G>A (n.2429+20G>A)
gnomAD v4
14g.23396265C=CA2123417753MYH6c.2429+19G= (n.2429+19G=)
14g.23396265C>TCA7115470MYH6c.2429+19G>A (n.2429+19G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396266C>ACA2503564646MYH6c.2429+18G>T (n.2429+18G>T)
gnomAD v4
14g.23396266C=CA2123417757MYH6c.2429+18G= (n.2429+18G=)
14g.23396266C>TCA7115471MYH6c.2429+18G>A (n.2429+18G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396268T>CCA704273085MYH6c.2429+16A>G (n.2429+16A>G)
dbSNP
14g.23396268T=CA2123417761MYH6c.2429+16A= (n.2429+16A=)
14g.23396269T>CCA2624246098MYH6c.2429+15A>G (n.2429+15A>G)
gnomAD v4
14g.23396269_23396272delinsTTCCCA2123417765MYH6c.2429+12_2429+15delinsGGAA (n.2429+12_2429+15delinsGGAA)
14g.23396270T>GCA134276MYH6c.2429+14A>C (n.2429+14A>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396270T=CA2123417768MYH6c.2429+14A= (n.2429+14A=)
14g.23396274_23396276delCA612933794MYH6c.2429+12_2429+14del (n.2429+12_2429+14del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396271C>TCA2624246109MYH6c.2429+13G>A (n.2429+13G>A)
gnomAD v4
14g.23396272C>TCA2624246111MYH6c.2429+12G>A (n.2429+12G>A)
gnomAD v4
14g.23396274C=CA2123417772MYH6c.2429+10G= (n.2429+10G=)
14g.23396274C>TCA7115472MYH6c.2429+10G>A (n.2429+10G>A)
dbSNP ExAC gnomAD v2
14g.23396275C=CA2123417773MYH6c.2429+9G= (n.2429+9G=)
14g.23396275C>TCA2123417774MYH6c.2429+9G>A (n.2429+9G>A)
dbSNP
14g.23396277G>ACA7115473MYH6c.2429+7C>T (n.2429+7C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396277G=CA2123417776MYH6c.2429+7C= (n.2429+7C=)
14g.23396278T>CCA2123417780MYH6c.2429+6A>G (n.2429+6A>G)
dbSNP
14g.23396278T=CA2123417779MYH6c.2429+6A= (n.2429+6A=)
14g.23396279C>GCA645591506MYH6c.2429+5G>C (n.2429+5G>C)
gnomAD v4 COSMIC
14g.23396281C=CA2123417781MYH6c.2429+3G= (n.2429+3G=)
14g.23396281C>TCA257789101MYH6c.2429+3G>A (n.2429+3G>A)
dbSNP
14g.23396282A>CCA389016003MYH6c.2429+2T>G (n.2429+2T>G)
14g.23396282A>GCA389016004MYH6c.2429+2T>C (n.2429+2T>C)
14g.23396282A>TCA389016006MYH6c.2429+2T>A (n.2429+2T>A)
14g.23396283C>ACA389016008MYH6c.2429+1G>T (n.2429+1G>T)
COSMIC
14g.23396283C>GCA389016009MYH6c.2429+1G>C (n.2429+1G>C)
14g.23396283C>TCA389016011MYH6c.2429+1G>A (n.2429+1G>A)
gnomAD v4
14g.23396284C>ACA389016014MYH6c.2429G>T (p.Arg810Met)
14g.23396284C>GCA389016015MYH6c.2429G>C (p.Arg810Thr)
14g.23396284C>TCA389016012MYH6c.2429G>A (p.Arg810Lys)
gnomAD v4
14g.23396285T>ACA389016017MYH6c.2428A>T (p.Arg810Trp)
dbSNP
14g.23396285T>CCA16614077MYH6c.2428A>G (p.Arg810Gly)
ClinVar dbSNP gnomAD v4
14g.23396285T>GCA485609907MYH6c.2428A>C (p.Arg810=)
14g.23396285T=CA2123417785MYH6c.2428A= (p.Arg810=)
14g.23396286G>ACA485609910MYH6c.2427C>T (p.Arg809=)
gnomAD v4
14g.23396286G>CCA485609909MYH6c.2427C>G (p.Arg809=)
14g.23396286G>TCA485609908MYH6c.2427C>A (p.Arg809=)
14g.23396287C>ACA389016020MYH6c.2426G>T (p.Arg809Leu)
14g.23396287C=CA2123417794MYH6c.2426G= (p.Arg809=)
14g.23396287C>GCA389016021MYH6c.2426G>C (p.Arg809Pro)
14g.23396287C>TCA7115474MYH6c.2426G>A (p.Arg809His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23396288G>ACA7115475MYH6c.2425C>T (p.Arg809Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396288G>CCA389016024MYH6c.2425C>G (p.Arg809Gly)
dbSNP gnomAD v2 gnomAD v4
14g.23396288G=CA2123417804MYH6c.2425C= (p.Arg809=)
14g.23396288G>TCA389016026MYH6c.2425C>A (p.Arg809Ser)
14g.23396289T>ACA389016027MYH6c.2424A>T (p.Glu808Asp)
14g.23396289T>CCA485609911MYH6c.2424A>G (p.Glu808=)
dbSNP
14g.23396289T>GCA389016029MYH6c.2424A>C (p.Glu808Asp)
14g.23396289T=CA2123417811MYH6c.2424A= (p.Glu808=)
14g.23396290T>ACA389016031MYH6c.2423A>T (p.Glu808Val)
14g.23396290T>CCA389016033MYH6c.2423A>G (p.Glu808Gly)
14g.23396290T>GCA389016034MYH6c.2423A>C (p.Glu808Ala)
14g.23396291C>ACA389016036MYH6c.2422G>T (p.Glu808Ter)
14g.23396291C=CA2123417816MYH6c.2422G= (p.Glu808=)
14g.23396291C>GCA389016040MYH6c.2422G>C (p.Glu808Gln)
14g.23396291C>TCA389016038MYH6c.2422G>A (p.Glu808Lys)
dbSNP gnomAD v4
14g.23396292C>ACA485609912MYH6c.2421G>T (p.Val807=)
14g.23396292C=CA2123417821MYH6c.2421G= (p.Val807=)
14g.23396292C>GCA485609913MYH6c.2421G>C (p.Val807=)
14g.23396292C>TCA7115476MYH6c.2421G>A (p.Val807=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396293A>CCA389016042MYH6c.2420T>G (p.Val807Gly)
gnomAD v4
14g.23396293A>GCA389016044MYH6c.2420T>C (p.Val807Ala)
14g.23396293A>TCA389016046MYH6c.2420T>A (p.Val807Glu)
14g.23396294C>ACA389016048MYH6c.2419G>T (p.Val807Leu)
ClinVar
14g.23396294C>GCA389016050MYH6c.2419G>C (p.Val807Leu)
ClinVar
14g.23396294C>TCA389016052MYH6c.2419G>A (p.Val807Met)
14g.23396295T>ACA7115477MYH6c.2418A>T (p.Ile806=)
dbSNP ExAC gnomAD v2
14g.23396295T>CCA389016054MYH6c.2418A>G (p.Ile806Met)
dbSNP
14g.23396295T>GCA485609914MYH6c.2418A>C (p.Ile806=)
14g.23396295T=CA2123417826MYH6c.2418A= (p.Ile806=)
14g.23396296A=CA2123417832MYH6c.2417T= (p.Ile806=)
14g.23396296A>CCA389016056MYH6c.2417T>G (p.Ile806Arg)
14g.23396296A>GCA389016058MYH6c.2417T>C (p.Ile806Thr)
dbSNP gnomAD v2 gnomAD v4
14g.23396296A>TCA389016059MYH6c.2417T>A (p.Ile806Lys)
14g.23396297T>ACA389016061MYH6c.2416A>T (p.Ile806Leu)
14g.23396297T>CCA389016062MYH6c.2416A>G (p.Ile806Val)
14g.23396297T>GCA389016064MYH6c.2416A>C (p.Ile806Leu)
14g.23396301_23396303delCA2624246190MYH6c.2414_2416del (p.Lys805del)
gnomAD v4
14g.23396298C>ACA389016067MYH6c.2415G>T (p.Lys805Asn)
14g.23396298C>GCA389016065MYH6c.2415G>C (p.Lys805Asn)
14g.23396298C>TCA485609915MYH6c.2415G>A (p.Lys805=)
14g.23396299T>ACA389016069MYH6c.2414A>T (p.Lys805Met)
14g.23396299T>CCA389016070MYH6c.2414A>G (p.Lys805Arg)
dbSNP
14g.23396299T>GCA389016072MYH6c.2414A>C (p.Lys805Thr)
14g.23396299T=CA2123417834MYH6c.2414A= (p.Lys805=)
14g.23396300T>ACA389016073MYH6c.2413A>T (p.Lys805Ter)
14g.23396300T>CCA389016074MYH6c.2413A>G (p.Lys805Glu)
14g.23396300T>GCA389016076MYH6c.2413A>C (p.Lys805Gln)
14g.23396301C>ACA389016079MYH6c.2412G>T (p.Lys804Asn)
COSMIC
14g.23396301C>GCA389016077MYH6c.2412G>C (p.Lys804Asn)
14g.23396301C>TCA485609916MYH6c.2412G>A (p.Lys804=)
14g.23396302T>ACA389016080MYH6c.2411A>T (p.Lys804Met)
14g.23396302T>CCA389016082MYH6c.2411A>G (p.Lys804Arg)
ClinVar gnomAD v4
14g.23396302T>GCA389016083MYH6c.2411A>C (p.Lys804Thr)
14g.23396303T>ACA389016085MYH6c.2410A>T (p.Lys804Ter)
14g.23396303T>CCA389016087MYH6c.2410A>G (p.Lys804Glu)
14g.23396303T>GCA389016088MYH6c.2410A>C (p.Lys804Gln)
dbSNP gnomAD v4
14g.23396303T=CA2123417837MYH6c.2410A= (p.Lys804=)
14g.23396304G>ACA257789145MYH6c.2409C>T (p.Phe803=)
dbSNP gnomAD v4
14g.23396304G>CCA389016093MYH6c.2409C>G (p.Phe803Leu)
dbSNP
14g.23396304G=CA2123417843MYH6c.2409C= (p.Phe803=)
14g.23396304G>TCA389016091MYH6c.2409C>A (p.Phe803Leu)
14g.23396305A>CCA389016094MYH6c.2408T>G (p.Phe803Cys)
14g.23396305A>GCA389016096MYH6c.2408T>C (p.Phe803Ser)
14g.23396305A>TCA389016098MYH6c.2408T>A (p.Phe803Tyr)
14g.23396306A>CCA389016100MYH6c.2407T>G (p.Phe803Val)
14g.23396306A>GCA389016101MYH6c.2407T>C (p.Phe803Leu)
ClinVar gnomAD v4
14g.23396306A>TCA389016103MYH6c.2407T>A (p.Phe803Ile)
14g.23396307C>ACA389016105MYH6c.2406G>T (p.Glu802Asp)
14g.23396307C=CA2123417845MYH6c.2406G= (p.Glu802=)
14g.23396307C>GCA389016107MYH6c.2406G>C (p.Glu802Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23396307C>TCA485609917MYH6c.2406G>A (p.Glu802=)
dbSNP gnomAD v4
14g.23396308T>ACA389016108MYH6c.2405A>T (p.Glu802Val)
14g.23396308T>CCA389016110MYH6c.2405A>G (p.Glu802Gly)
14g.23396308T>GCA389016112MYH6c.2405A>C (p.Glu802Ala)
14g.23396309C>ACA389016114MYH6c.2404G>T (p.Glu802Ter)
14g.23396309C>GCA389016115MYH6c.2404G>C (p.Glu802Gln)
14g.23396309C>TCA389016117MYH6c.2404G>A (p.Glu802Lys)
14g.23396310A>CCA389016119MYH6c.2403T>G (p.Ile801Met)
14g.23396310A>GCA485609919MYH6c.2403T>C (p.Ile801=)
14g.23396310A>TCA485609920MYH6c.2403T>A (p.Ile801=)
14g.23396311A=CA2123417847MYH6c.2402T= (p.Ile801=)
14g.23396311A>CCA389016121MYH6c.2402T>G (p.Ile801Ser)
14g.23396311A>GCA389016122MYH6c.2402T>C (p.Ile801Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23396311A>TCA389016123MYH6c.2402T>A (p.Ile801Asn)
14g.23396312T>ACA7115478MYH6c.2401A>T (p.Ile801Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396312T>CCA134273MYH6c.2401A>G (p.Ile801Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396312T>GCA389016126MYH6c.2401A>C (p.Ile801Leu)
dbSNP gnomAD v4
14g.23396312T=CA2123417853MYH6c.2401A= (p.Ile801=)
14g.23396313G>ACA485609922MYH6c.2400C>T (p.Arg800=)
14g.23396313G>CCA485609923MYH6c.2400C>G (p.Arg800=)
14g.23396313G>TCA485609924MYH6c.2400C>A (p.Arg800=)
14g.23396316_23396350delCA2624246239MYH6c.2366_2400del (p.Arg789HisfsTer2)
gnomAD v4
14g.23396314C>ACA389016128MYH6c.2399G>T (p.Arg800Leu)
ClinVar dbSNP gnomAD v4
14g.23396314C=CA2123417863MYH6c.2399G= (p.Arg800=)
14g.23396314C>GCA389016129MYH6c.2399G>C (p.Arg800Pro)
14g.23396314C>TCA7115479MYH6c.2399G>A (p.Arg800His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396315G>ACA7115480MYH6c.2398C>T (p.Arg800Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23396315G>CCA389016133MYH6c.2398C>G (p.Arg800Gly)
14g.23396315G=CA2123417872MYH6c.2398C= (p.Arg800=)
14g.23396315G>TCA7115481MYH6c.2398C>A (p.Arg800Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396316C>ACA389016138MYH6c.2397G>T (p.Met799Ile)
14g.23396316C=CA2123417873MYH6c.2397G= (p.Met799=)
14g.23396316C>GCA389016135MYH6c.2397G>C (p.Met799Ile)
14g.23396316C>TCA7115482MYH6c.2397G>A (p.Met799Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396317A=CA2123417878MYH6c.2396T= (p.Met799=)
14g.23396317A>CCA389016140MYH6c.2396T>G (p.Met799Arg)
14g.23396317A>GCA389016145MYH6c.2396T>C (p.Met799Thr)
ClinVar dbSNP gnomAD v4
14g.23396317A>TCA389016141MYH6c.2396T>A (p.Met799Lys)
14g.23396318T>ACA257789167MYH6c.2395A>T (p.Met799Leu)
dbSNP
14g.23396318T>CCA389016147MYH6c.2395A>G (p.Met799Val)
gnomAD v4
14g.23396318T>GCA389016148MYH6c.2395A>C (p.Met799Leu)
14g.23396318T=CA2123417886MYH6c.2395A= (p.Met799=)
14g.23396319G>ACA485609929MYH6c.2394C>T (p.Leu798=)
COSMIC
14g.23396319G>CCA485609930MYH6c.2394C>G (p.Leu798=)
14g.23396319G>TCA485609931MYH6c.2394C>A (p.Leu798=)
14g.23396320A>CCA389016150MYH6c.2393T>G (p.Leu798Arg)
gnomAD v4 COSMIC
14g.23396320A>GCA389016152MYH6c.2393T>C (p.Leu798Pro)
14g.23396320A>TCA389016153MYH6c.2393T>A (p.Leu798His)
14g.23396321G>ACA389016156MYH6c.2392C>T (p.Leu798Phe)
14g.23396321G>CCA389016157MYH6c.2392C>G (p.Leu798Val)
14g.23396321G>TCA389016159MYH6c.2392C>A (p.Leu798Ile)
14g.23396322C>ACA389016160MYH6c.2391G>T (p.Gln797His)
14g.23396322C=CA2123417890MYH6c.2391G= (p.Gln797=)
14g.23396322C>GCA389016162MYH6c.2391G>C (p.Gln797His)
14g.23396322C>TCA485609934MYH6c.2391G>A (p.Gln797=)
dbSNP gnomAD v2 gnomAD v4
14g.23396323T>ACA389016167MYH6c.2390A>T (p.Gln797Leu)
14g.23396323T>CCA389016166MYH6c.2390A>G (p.Gln797Arg)
14g.23396323T>GCA389016164MYH6c.2390A>C (p.Gln797Pro)
14g.23396324G>ACA389016170MYH6c.2389C>T (p.Gln797Ter)
14g.23396324G>CCA389016172MYH6c.2389C>G (p.Gln797Glu)
14g.23396324G>TCA389016173MYH6c.2389C>A (p.Gln797Lys)
14g.23396325G>ACA485609936MYH6c.2388C>T (p.Gly796=)
14g.23396325G>CCA485609937MYH6c.2388C>G (p.Gly796=)
14g.23396325G>TCA485609938MYH6c.2388C>A (p.Gly796=)
ClinVar
14g.23396326C>ACA389016176MYH6c.2387G>T (p.Gly796Val)
14g.23396326C>GCA389016178MYH6c.2387G>C (p.Gly796Ala)
14g.23396326C>TCA389016180MYH6c.2387G>A (p.Gly796Asp)
14g.23396327C>ACA389016183MYH6c.2386G>T (p.Gly796Cys)
14g.23396327C>GCA389016184MYH6c.2386G>C (p.Gly796Arg)
14g.23396327C>TCA389016186MYH6c.2386G>A (p.Gly796Ser)
14g.23396328C>ACA485609941MYH6c.2385G>T (p.Arg795=)
14g.23396328C=CA2123417894MYH6c.2385G= (p.Arg795=)
14g.23396328C>GCA485609942MYH6c.2385G>C (p.Arg795=)
COSMIC
14g.23396328C>TCA485609943MYH6c.2385G>A (p.Arg795=)
dbSNP gnomAD v4
14g.23396329C>ACA389016189MYH6c.2384G>T (p.Arg795Leu)
14g.23396329C=CA2123417897MYH6c.2384G= (p.Arg795=)
14g.23396329C>GCA389016190MYH6c.2384G>C (p.Arg795Pro)
gnomAD v4
14g.23396329C>TCA123764MYH6c.2384G>A (p.Arg795Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396330G>ACA7115483MYH6c.2383C>T (p.Arg795Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396330G>CCA389016194MYH6c.2383C>G (p.Arg795Gly)
14g.23396330G=CA2123417903MYH6c.2383C= (p.Arg795=)
14g.23396330G>TCA485609947MYH6c.2383C>A (p.Arg795=)
gnomAD v4
14g.23396331G>ACA485609948MYH6c.2382C>T (p.Ala794=)
14g.23396331G>CCA485609949MYH6c.2382C>G (p.Ala794=)
14g.23396331G>TCA485609950MYH6c.2382C>A (p.Ala794=)
14g.23396332G>ACA389016197MYH6c.2381C>T (p.Ala794Val)
gnomAD v4
14g.23396332G>CCA389016198MYH6c.2381C>G (p.Ala794Gly)
14g.23396332G>TCA389016200MYH6c.2381C>A (p.Ala794Asp)
14g.23396333C>ACA389016202MYH6c.2380G>T (p.Ala794Ser)
14g.23396333C>GCA389016203MYH6c.2380G>C (p.Ala794Pro)
14g.23396333C>TCA389016205MYH6c.2380G>A (p.Ala794Thr)
14g.23396334T>ACA389016209MYH6c.2379A>T (p.Gln793His)
14g.23396334T>CCA7115484MYH6c.2379A>G (p.Gln793=)
ClinVar dbSNP ExAC gnomAD v4 COSMIC
14g.23396334T>GCA389016207MYH6c.2379A>C (p.Gln793His)
14g.23396334T=CA2123417911MYH6c.2379A= (p.Gln793=)
14g.23396335T>ACA389016212MYH6c.2378A>T (p.Gln793Leu)
14g.23396335T>CCA389016213MYH6c.2378A>G (p.Gln793Arg)
14g.23396335T>GCA389016214MYH6c.2378A>C (p.Gln793Pro)
14g.23396336G>ACA389016217MYH6c.2377C>T (p.Gln793Ter)
gnomAD v4
14g.23396336G>CCA389016218MYH6c.2377C>G (p.Gln793Glu)
14g.23396336G>TCA389016220MYH6c.2377C>A (p.Gln793Lys)
gnomAD v4
14g.23396337G>ACA485609955MYH6c.2376C>T (p.Ala792=)
dbSNP
14g.23396337G>CCA485609954MYH6c.2376C>G (p.Ala792=)
14g.23396337G=CA2123417915MYH6c.2376C= (p.Ala792=)
14g.23396337G>TCA485609953MYH6c.2376C>A (p.Ala792=)
14g.23396338G>ACA389016222MYH6c.2375C>T (p.Ala792Val)
14g.23396338G>CCA389016224MYH6c.2375C>G (p.Ala792Gly)
14g.23396338G>TCA389016223MYH6c.2375C>A (p.Ala792Asp)
14g.23396339C>ACA389016225MYH6c.2374G>T (p.Ala792Ser)
14g.23396339C>GCA389016227MYH6c.2374G>C (p.Ala792Pro)
14g.23396339C>TCA389016229MYH6c.2374G>A (p.Ala792Thr)
ClinVar
14g.23396340C>ACA389016231MYH6c.2373G>T (p.Gln791His)
dbSNP
14g.23396340C=CA2123417918MYH6c.2373G= (p.Gln791=)
14g.23396340C>GCA389016232MYH6c.2373G>C (p.Gln791His)
14g.23396340C>TCA485609958MYH6c.2373G>A (p.Gln791=)

Number of alleles fetched