Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23396301_23396303delCA2624246190MYH6c.2414_2416del (p.Lys805del)
gnomAD v4
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=)
14g.23396341T>ACA389016234MYH6c.2372A>T (p.Gln791Leu)
14g.23396341T>CCA389016236MYH6c.2372A>G (p.Gln791Arg)
gnomAD v4
14g.23396341T>GCA389016238MYH6c.2372A>C (p.Gln791Pro)
14g.23396342G>ACA257789181MYH6c.2371C>T (p.Gln791Ter)
dbSNP gnomAD v2 gnomAD v4
14g.23396342G>CCA7115485MYH6c.2371C>G (p.Gln791Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396342G=CA2123417924MYH6c.2371C= (p.Gln791=)
14g.23396342G>TCA389016241MYH6c.2371C>A (p.Gln791Lys)
14g.23396343C>ACA389016243MYH6c.2370G>T (p.Met790Ile)
14g.23396343C=CA2123417928MYH6c.2370G= (p.Met790=)
14g.23396343C>GCA389016246MYH6c.2370G>C (p.Met790Ile)
dbSNP
14g.23396343C>TCA389016244MYH6c.2370G>A (p.Met790Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396344A=CA2123417931MYH6c.2369T= (p.Met790=)
14g.23396344A>CCA389016248MYH6c.2369T>G (p.Met790Arg)
14g.23396344A>GCA389016251MYH6c.2369T>C (p.Met790Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23396344A>TCA389016250MYH6c.2369T>A (p.Met790Lys)
14g.23396345T>ACA7115486MYH6c.2368A>T (p.Met790Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396345T>CCA10576947MYH6c.2368A>G (p.Met790Val)
ClinVar dbSNP gnomAD v4
14g.23396345T>GCA389016254MYH6c.2368A>C (p.Met790Leu)
ClinVar gnomAD v4
14g.23396345T=CA2123417932MYH6c.2368A= (p.Met790=)
14g.23396346G>ACA485609963MYH6c.2367C>T (p.Arg789=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396346G>CCA485609965MYH6c.2367C>G (p.Arg789=)
14g.23396346G=CA2123417933MYH6c.2367C= (p.Arg789=)
14g.23396346G>TCA485609966MYH6c.2367C>A (p.Arg789=)
dbSNP
14g.23396347C>ACA389016256MYH6c.2366G>T (p.Arg789Leu)
gnomAD v4
14g.23396347C=CA2123417934MYH6c.2366G= (p.Arg789=)
14g.23396347C>GCA389016257MYH6c.2366G>C (p.Arg789Pro)
14g.23396347C>TCA7115487MYH6c.2366G>A (p.Arg789His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23396348G>ACA7115488MYH6c.2365C>T (p.Arg789Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23396348G>CCA389016261MYH6c.2365C>G (p.Arg789Gly)
14g.23396348G=CA2123417935MYH6c.2365C= (p.Arg789=)
14g.23396348G>TCA389016262MYH6c.2365C>A (p.Arg789Ser)
dbSNP
14g.23396349C>ACA485609969MYH6c.2364G>T (p.Thr788=)
14g.23396349C=CA2123417936MYH6c.2364G= (p.Thr788=)
14g.23396349C>GCA485609971MYH6c.2364G>C (p.Thr788=)
dbSNP
14g.23396349C>TCA7115489MYH6c.2364G>A (p.Thr788=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23396350G>ACA7115490MYH6c.2363C>T (p.Thr788Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396350G>CCA7115491MYH6c.2363C>G (p.Thr788Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396350G=CA2123417938MYH6c.2363C= (p.Thr788=)
14g.23396350G>TCA389016266MYH6c.2363C>A (p.Thr788Lys)
gnomAD v4
14g.23396351T>ACA389016271MYH6c.2362A>T (p.Thr788Ser)
14g.23396351T>CCA389016270MYH6c.2362A>G (p.Thr788Ala)
14g.23396351T>GCA389016268MYH6c.2362A>C (p.Thr788Pro)
14g.23396352G>ACA485609976MYH6c.2361C>T (p.Ile787=)
14g.23396352G>CCA389016273MYH6c.2361C>G (p.Ile787Met)
ClinVar dbSNP
14g.23396352G=CA2123417940MYH6c.2361C= (p.Ile787=)
14g.23396352G>TCA485609977MYH6c.2361C>A (p.Ile787=)
14g.23396353A=CA2123417942MYH6c.2360T= (p.Ile787=)
14g.23396353A>CCA389016275MYH6c.2360T>G (p.Ile787Ser)
14g.23396353A>GCA389016277MYH6c.2360T>C (p.Ile787Thr)
dbSNP gnomAD v3 gnomAD v4
14g.23396353A>TCA389016278MYH6c.2360T>A (p.Ile787Asn)
14g.23396354T>ACA389016280MYH6c.2359A>T (p.Ile787Phe)
14g.23396354T>CCA389016281MYH6c.2359A>G (p.Ile787Val)
ClinVar dbSNP gnomAD v2
14g.23396354T>GCA389016283MYH6c.2359A>C (p.Ile787Leu)
14g.23396354T=CA2123417945MYH6c.2359A= (p.Ile787=)
14g.23396355G>ACA485609979MYH6c.2358C>T (p.Ile786=)
14g.23396355G>CCA389016284MYH6c.2358C>G (p.Ile786Met)
14g.23396355G>TCA485609980MYH6c.2358C>A (p.Ile786=)
14g.23396356A=CA2123417948MYH6c.2357T= (p.Ile786=)
14g.23396356A>CCA7115492MYH6c.2357T>G (p.Ile786Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396356A>GCA389016286MYH6c.2357T>C (p.Ile786Thr)
14g.23396356A>TCA7115493MYH6c.2357T>A (p.Ile786Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396357T>ACA389016290MYH6c.2356A>T (p.Ile786Phe)
14g.23396357T>CCA389016288MYH6c.2356A>G (p.Ile786Val)
14g.23396357T>GCA389016287MYH6c.2356A>C (p.Ile786Leu)
14g.23396358G>ACA485609981MYH6c.2355C>T (p.Arg785=)
14g.23396358G>CCA485609982MYH6c.2355C>G (p.Arg785=)
dbSNP
14g.23396358G=CA2123417952MYH6c.2355C= (p.Arg785=)
14g.23396358G>TCA257789235MYH6c.2355C>A (p.Arg785=)
dbSNP gnomAD v4
14g.23396359C>ACA389016293MYH6c.2354G>T (p.Arg785Leu)
gnomAD v4 COSMIC
14g.23396359C=CA2123417960MYH6c.2354G= (p.Arg785=)
14g.23396359C>GCA389016294MYH6c.2354G>C (p.Arg785Pro)
14g.23396359C>TCA7115494MYH6c.2354G>A (p.Arg785His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396360G>ACA7115495MYH6c.2353C>T (p.Arg785Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23396360G>CCA389016297MYH6c.2353C>G (p.Arg785Gly)
14g.23396360G=CA2123417964MYH6c.2353C= (p.Arg785=)
14g.23396360G>TCA389016299MYH6c.2353C>A (p.Arg785Ser)
14g.23396361G>ACA485609988MYH6c.2352C>T (p.Ser784=)
14g.23396361G>CCA389016300MYH6c.2352C>G (p.Ser784Arg)
14g.23396361G>TCA389016302MYH6c.2352C>A (p.Ser784Arg)
14g.23396362C>ACA389016304MYH6c.2351G>T (p.Ser784Ile)
14g.23396362C>GCA389016305MYH6c.2351G>C (p.Ser784Thr)
14g.23396362C>TCA389016307MYH6c.2351G>A (p.Ser784Asn)
gnomAD v4
14g.23396363T>ACA389016313MYH6c.2350A>T (p.Ser784Cys)
gnomAD v4
14g.23396363T>CCA389016309MYH6c.2350A>G (p.Ser784Gly)
14g.23396363T>GCA389016311MYH6c.2350A>C (p.Ser784Arg)
14g.23396363_23396364delinsTCCA2123417973MYH6c.2349_2350delinsGA (p.Leu783=)
14g.23396364delCA612933836MYH6c.2349del (p.Ser784AlafsTer23)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396364C>ACA485609992MYH6c.2349G>T (p.Leu783=)
14g.23396364C>GCA485609995MYH6c.2349G>C (p.Leu783=)
14g.23396364C>TCA485609996MYH6c.2349G>A (p.Leu783=)
14g.23396365A>CCA389016314MYH6c.2348T>G (p.Leu783Arg)
14g.23396365A>GCA389016316MYH6c.2348T>C (p.Leu783Pro)
14g.23396365A>TCA389016317MYH6c.2348T>A (p.Leu783Gln)
14g.23396366G>ACA485609998MYH6c.2347C>T (p.Leu783=)
dbSNP gnomAD v3 gnomAD v4
14g.23396366G>CCA389016319MYH6c.2347C>G (p.Leu783Val)
14g.23396366G=CA2123417979MYH6c.2347C= (p.Leu783=)
14g.23396366G>TCA257789241MYH6c.2347C>A (p.Leu783Met)
dbSNP
14g.23396367C>ACA389016321MYH6c.2346G>T (p.Arg782Ser)
14g.23396367C>GCA389016323MYH6c.2346G>C (p.Arg782Ser)
14g.23396367C>TCA485610001MYH6c.2346G>A (p.Arg782=)
14g.23396368C>ACA389016325MYH6c.2345G>T (p.Arg782Met)
14g.23396368C=CA2123417983MYH6c.2345G= (p.Arg782=)
14g.23396368C>GCA389016326MYH6c.2345G>C (p.Arg782Thr)
14g.23396368C>TCA257789243MYH6c.2345G>A (p.Arg782Lys)
dbSNP gnomAD v3 gnomAD v4
14g.23396369T>ACA389016329MYH6c.2344A>T (p.Arg782Trp)
14g.23396369T>CCA389016330MYH6c.2344A>G (p.Arg782Gly)
dbSNP gnomAD v2 gnomAD v4
14g.23396369T>GCA485610003MYH6c.2344A>C (p.Arg782=)
14g.23396369T=CA2123417987MYH6c.2344A= (p.Arg782=)
14g.23396370C>ACA389016333MYH6c.2343G>T (p.Glu781Asp)
14g.23396370C=CA2123417990MYH6c.2343G= (p.Glu781=)
14g.23396370C>GCA389016332MYH6c.2343G>C (p.Glu781Asp)
dbSNP gnomAD v2 gnomAD v4
14g.23396370C>TCA485610004MYH6c.2343G>A (p.Glu781=)
14g.23396371T>ACA389016335MYH6c.2342A>T (p.Glu781Val)
14g.23396371T>CCA389016337MYH6c.2342A>G (p.Glu781Gly)
14g.23396371T>GCA389016339MYH6c.2342A>C (p.Glu781Ala)
14g.23396372C>ACA389016340MYH6c.2341G>T (p.Glu781Ter)
14g.23396372C>GCA389016342MYH6c.2341G>C (p.Glu781Gln)
14g.23396372C>TCA389016344MYH6c.2341G>A (p.Glu781Lys)
14g.23396373A>CCA389016347MYH6c.2340T>G (p.Asp780Glu)
14g.23396373A>GCA485610007MYH6c.2340T>C (p.Asp780=)
14g.23396373A>TCA389016346MYH6c.2340T>A (p.Asp780Glu)
14g.23396374T>ACA389016349MYH6c.2339A>T (p.Asp780Val)
14g.23396374T>CCA389016351MYH6c.2339A>G (p.Asp780Gly)
14g.23396374T>GCA389016352MYH6c.2339A>C (p.Asp780Ala)
14g.23396375C>ACA389016354MYH6c.2338G>T (p.Asp780Tyr)
14g.23396375C=CA2123417993MYH6c.2338G= (p.Asp780=)
14g.23396375C>GCA389016355MYH6c.2338G>C (p.Asp780His)
14g.23396375C>TCA7115496MYH6c.2338G>A (p.Asp780Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396376C>ACA485610012MYH6c.2337G>T (p.Arg779=)
14g.23396376C=CA2123417996MYH6c.2337G= (p.Arg779=)
14g.23396376C>GCA485610013MYH6c.2337G>C (p.Arg779=)
14g.23396376C>TCA485610015MYH6c.2337G>A (p.Arg779=)
dbSNP
14g.23396377C>ACA389016361MYH6c.2336G>T (p.Arg779Leu)
14g.23396377C=CA2123418000MYH6c.2336G= (p.Arg779=)
14g.23396377C>GCA389016358MYH6c.2336G>C (p.Arg779Pro)
14g.23396377C>TCA389016360MYH6c.2336G>A (p.Arg779Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396378G>ACA7115497MYH6c.2335C>T (p.Arg779Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23396378G>CCA389016364MYH6c.2335C>G (p.Arg779Gly)
14g.23396378G=CA2123418003MYH6c.2335C= (p.Arg779=)
14g.23396378G>TCA485610016MYH6c.2335C>A (p.Arg779=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396379C>ACA389016366MYH6c.2334G>T (p.Met778Ile)
14g.23396379C=CA2123418004MYH6c.2334G= (p.Met778=)
14g.23396379C>GCA389016367MYH6c.2334G>C (p.Met778Ile)
dbSNP gnomAD v2 gnomAD v4
14g.23396379C>TCA389016369MYH6c.2334G>A (p.Met778Ile)
ClinVar
14g.23396380A>CCA389016371MYH6c.2333T>G (p.Met778Arg)
14g.23396380A>GCA389016373MYH6c.2333T>C (p.Met778Thr)
14g.23396380A>TCA389016374MYH6c.2333T>A (p.Met778Lys)
14g.23396381T>ACA7115498MYH6c.2332A>T (p.Met778Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23396381T>CCA389016377MYH6c.2332A>G (p.Met778Val)
COSMIC
14g.23396381T>GCA389016378MYH6c.2332A>C (p.Met778Leu)
14g.23396381T=CA2123418005MYH6c.2332A= (p.Met778=)
14g.23396382C>ACA389016380MYH6c.2331G>T (p.Glu777Asp)
14g.23396382C>GCA389016382MYH6c.2331G>C (p.Glu777Asp)
14g.23396382C>TCA485610018MYH6c.2331G>A (p.Glu777=)
COSMIC
14g.23396383T>ACA389016384MYH6c.2330A>T (p.Glu777Val)
14g.23396383T>CCA389016388MYH6c.2330A>G (p.Glu777Gly)
14g.23396383T>GCA389016386MYH6c.2330A>C (p.Glu777Ala)
dbSNP
14g.23396384C>ACA389016390MYH6c.2329G>T (p.Glu777Ter)
14g.23396384C=CA2123418007MYH6c.2329G= (p.Glu777=)
14g.23396384C>GCA389016391MYH6c.2329G>C (p.Glu777Gln)
14g.23396384C>TCA7115499MYH6c.2329G>A (p.Glu777Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
14g.23396385C>ACA389016393MYH6c.2328G>T (p.Glu776Asp)
14g.23396385C>GCA389016395MYH6c.2328G>C (p.Glu776Asp)
14g.23396385C>TCA485610021MYH6c.2328G>A (p.Glu776=)
14g.23396386T>ACA389016397MYH6c.2327A>T (p.Glu776Val)
14g.23396386T>CCA389016399MYH6c.2327A>G (p.Glu776Gly)
14g.23396386T>GCA389016400MYH6c.2327A>C (p.Glu776Ala)
14g.23396387C>ACA389016402MYH6c.2326G>T (p.Glu776Ter)
14g.23396387C>GCA389016404MYH6c.2326G>C (p.Glu776Gln)
14g.23396387C>TCA389016405MYH6c.2326G>A (p.Glu776Lys)
14g.23396388delCA2624246458MYH6c.2326del (p.Glu776ArgfsTer8)
gnomAD v4
14g.23396388C>ACA485610025MYH6c.2325G>T (p.Leu775=)
ClinVar dbSNP
14g.23396388C=CA2123418012MYH6c.2325G= (p.Leu775=)
14g.23396388C>GCA485610026MYH6c.2325G>C (p.Leu775=)
14g.23396388C>TCA485610027MYH6c.2325G>A (p.Leu775=)
14g.23396389A>CCA389016411MYH6c.2324T>G (p.Leu775Arg)
14g.23396389A>GCA389016409MYH6c.2324T>C (p.Leu775Pro)
14g.23396389A>TCA389016407MYH6c.2324T>A (p.Leu775Gln)
14g.23396390G>ACA485610031MYH6c.2323C>T (p.Leu775=)
14g.23396390G>CCA389016412MYH6c.2323C>G (p.Leu775Val)
14g.23396390G>TCA389016413MYH6c.2323C>A (p.Leu775Met)
14g.23396391C>ACA485610032MYH6c.2322G>T (p.Leu774=)
14g.23396391C=CA2123418016MYH6c.2322G= (p.Leu774=)
14g.23396391C>GCA485610033MYH6c.2322G>C (p.Leu774=)
14g.23396391C>TCA485610034MYH6c.2322G>A (p.Leu774=)
ClinVar dbSNP gnomAD v4
14g.23396392A=CA2123418023MYH6c.2321T= (p.Leu774=)
14g.23396392A>CCA389016416MYH6c.2321T>G (p.Leu774Arg)
14g.23396392A>GCA389016418MYH6c.2321T>C (p.Leu774Pro)
dbSNP gnomAD v2 gnomAD v4
14g.23396392A>TCA389016419MYH6c.2321T>A (p.Leu774Gln)
dbSNP
14g.23396393G>ACA485610036MYH6c.2320C>T (p.Leu774=)
dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23396393G>CCA389016421MYH6c.2320C>G (p.Leu774Val)
14g.23396393G=CA2123418026MYH6c.2320C= (p.Leu774=)
14g.23396393G>TCA389016423MYH6c.2320C>A (p.Leu774Met)
14g.23396394C>ACA485610037MYH6c.2319G>T (p.Gly773=)
14g.23396394C>GCA485610038MYH6c.2319G>C (p.Gly773=)
14g.23396394C>TCA485610040MYH6c.2319G>A (p.Gly773=)
14g.23396395C>ACA389016425MYH6c.2318G>T (p.Gly773Val)
14g.23396395C>GCA389016427MYH6c.2318G>C (p.Gly773Ala)
14g.23396395C>TCA389016428MYH6c.2318G>A (p.Gly773Glu)
14g.23396396C>ACA389016430MYH6c.2317G>T (p.Gly773Trp)
14g.23396396C>GCA389016431MYH6c.2317G>C (p.Gly773Arg)
14g.23396396C>TCA389016433MYH6c.2317G>A (p.Gly773Arg)
14g.23396397A=CA2123418029MYH6c.2316T= (p.Leu772=)
14g.23396397A>CCA485610041MYH6c.2316T>G (p.Leu772=)
dbSNP
14g.23396397A>GCA485610043MYH6c.2316T>C (p.Leu772=)
14g.23396397A>TCA485610045MYH6c.2316T>A (p.Leu772=)
14g.23396398A>CCA389016437MYH6c.2315T>G (p.Leu772Arg)
14g.23396398A>GCA389016439MYH6c.2315T>C (p.Leu772Pro)
14g.23396398A>TCA389016436MYH6c.2315T>A (p.Leu772His)
14g.23396399G>ACA389016443MYH6c.2314C>T (p.Leu772Phe)
14g.23396399G>CCA389016441MYH6c.2314C>G (p.Leu772Val)
14g.23396399G>TCA389016444MYH6c.2314C>A (p.Leu772Ile)
14g.23396400C>ACA7115500MYH6c.2313G>T (p.Leu771=)
dbSNP ExAC gnomAD v4
14g.23396400C=CA2123418033MYH6c.2313G= (p.Leu771=)
14g.23396400C>GCA485610048MYH6c.2313G>C (p.Leu771=)
14g.23396400C>TCA485610049MYH6c.2313G>A (p.Leu771=)
14g.23396401A=CA2123418039MYH6c.2312T= (p.Leu771=)
14g.23396401A>CCA389016447MYH6c.2312T>G (p.Leu771Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23396401A>GCA389016448MYH6c.2312T>C (p.Leu771Pro)
14g.23396401A>TCA389016449MYH6c.2312T>A (p.Leu771Gln)
14g.23396402G>ACA485610050MYH6c.2311C>T (p.Leu771=)
14g.23396402G>CCA389016450MYH6c.2311C>G (p.Leu771Val)
14g.23396402G=CA2123418043MYH6c.2311C= (p.Leu771=)
14g.23396402G>TCA257789262MYH6c.2311C>A (p.Leu771Met)
dbSNP gnomAD v3 gnomAD v4
14g.23396403C>ACA485610053MYH6c.2310G>T (p.Gly770=)
14g.23396403C=CA2123418047MYH6c.2310G= (p.Gly770=)
14g.23396403C>GCA485610052MYH6c.2310G>C (p.Gly770=)
14g.23396403C>TCA7115501MYH6c.2310G>A (p.Gly770=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched