Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23419258C>ACA485620098MYH7c.3891G>T (p.Leu1297=)
14g.23419258C>GCA485620100MYH7c.3891G>C (p.Leu1297=)
14g.23419258C>TCA485620102MYH7c.3891G>A (p.Leu1297=)
ClinVar dbSNP
14g.23419259A=CA2123444508MYH7c.3890T= (p.Leu1297=)
14g.23419259A>CCA389041693MYH7c.3890T>G (p.Leu1297Arg)
14g.23419259A>GCA389041691MYH7c.3890T>C (p.Leu1297Pro)
14g.23419259A>TCA389041689MYH7c.3890T>A (p.Leu1297Gln)
ClinVar dbSNP
14g.23419260G>ACA485620109MYH7c.3889C>T (p.Leu1297=)
dbSNP gnomAD v3 gnomAD v4
14g.23419260G>CCA389041694MYH7c.3889C>G (p.Leu1297Val)
14g.23419260G=CA2123444516MYH7c.3889C= (p.Leu1297=)
14g.23419260G>TCA389041696MYH7c.3889C>A (p.Leu1297Met)
COSMIC
14g.23419261T>ACA039417MYH7c.3888A>T (p.Ala1296=)
dbSNP ExAC gnomAD v2
14g.23419261T>CCA257814672MYH7c.3888A>G (p.Ala1296=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419261T>GCA485620113MYH7c.3888A>C (p.Ala1296=)
14g.23419261T=CA2123444522MYH7c.3888A= (p.Ala1296=)
14g.23419262G>ACA389041698MYH7c.3887C>T (p.Ala1296Val)
14g.23419262G>CCA389041700MYH7c.3887C>G (p.Ala1296Gly)
14g.23419262G>TCA389041701MYH7c.3887C>A (p.Ala1296Glu)
ClinVar
14g.23419263C>ACA389041703MYH7c.3886G>T (p.Ala1296Ser)
14g.23419263C=CA2123444530MYH7c.3886G= (p.Ala1296=)
14g.23419263C>GCA389041704MYH7c.3886G>C (p.Ala1296Pro)
14g.23419263C>TCA389041705MYH7c.3886G>A (p.Ala1296Thr)
dbSNP gnomAD v3 gnomAD v4
14g.23419264C>ACA389041707MYH7c.3885G>T (p.Glu1295Asp)
14g.23419264C>GCA389041709MYH7c.3885G>C (p.Glu1295Asp)
gnomAD v4
14g.23419264C>TCA485620121MYH7c.3885G>A (p.Glu1295=)
ClinVar dbSNP
14g.23419265T>ACA389041712MYH7c.3884A>T (p.Glu1295Val)
14g.23419265T>CCA389041713MYH7c.3884A>G (p.Glu1295Gly)
14g.23419265T>GCA389041710MYH7c.3884A>C (p.Glu1295Ala)
14g.23419266C>ACA389041714MYH7c.3883G>T (p.Glu1295Ter)
14g.23419266C=CA2123444543MYH7c.3883G= (p.Glu1295=)
14g.23419266C>GCA389041716MYH7c.3883G>C (p.Glu1295Gln)
14g.23419266C>TCA014200MYH7c.3883G>A (p.Glu1295Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419266_23419269delinsCCTTCA2123444550MYH7c.3880_3883delinsAAGG (p.Lys1294=)
14g.23419267C>ACA389041719MYH7c.3882G>T (p.Lys1294Asn)
ClinVar dbSNP
14g.23419267C=CA2123444562MYH7c.3882G= (p.Lys1294=)
14g.23419267C>GCA389041720MYH7c.3882G>C (p.Lys1294Asn)
14g.23419267C>TCA485620129MYH7c.3882G>A (p.Lys1294=)
ClinVar dbSNP gnomAD v4
14g.23419269_23419271delCA658798188MYH7c.3880_3882del (p.Lys1294del)
ClinVar dbSNP
14g.23419268T>ACA389041724MYH7c.3881A>T (p.Lys1294Met)
14g.23419268T>CCA389041721MYH7c.3881A>G (p.Lys1294Arg)
14g.23419268T>GCA389041722MYH7c.3881A>C (p.Lys1294Thr)
14g.23419269T>ACA389041725MYH7c.3880A>T (p.Lys1294Ter)
14g.23419269T>CCA389041726MYH7c.3880A>G (p.Lys1294Glu)
14g.23419269T>GCA389041727MYH7c.3880A>C (p.Lys1294Gln)
14g.23419270C>ACA389041729MYH7c.3879G>T (p.Glu1293Asp)
14g.23419270C>GCA389041730MYH7c.3879G>C (p.Glu1293Asp)
14g.23419270C>TCA485620138MYH7c.3879G>A (p.Glu1293=)
14g.23419271T>ACA389041735MYH7c.3878A>T (p.Glu1293Val)
14g.23419271T>CCA389041733MYH7c.3878A>G (p.Glu1293Gly)
14g.23419271T>GCA389041731MYH7c.3878A>C (p.Glu1293Ala)
14g.23419272C>ACA389041736MYH7c.3877G>T (p.Glu1293Ter)
14g.23419272C>GCA389041739MYH7c.3877G>C (p.Glu1293Gln)
14g.23419272C>TCA389041737MYH7c.3877G>A (p.Glu1293Lys)
ClinVar
14g.23419273_23419296delCA2575504245MYH7c.3854_3877del
14g.23419273A>CCA389041741MYH7c.3876T>G (p.Asp1292Glu)
14g.23419273A>GCA485620145MYH7c.3876T>C (p.Asp1292=)
14g.23419273A>TCA389041745MYH7c.3876T>A (p.Asp1292Glu)
14g.23419274T>ACA389041747MYH7c.3875A>T (p.Asp1292Val)
dbSNP
14g.23419274T>CCA389041748MYH7c.3875A>G (p.Asp1292Gly)
14g.23419274T>GCA389041750MYH7c.3875A>C (p.Asp1292Ala)
14g.23419274T=CA2123444566MYH7c.3875A= (p.Asp1292=)
14g.23419275C>ACA389041752MYH7c.3874G>T (p.Asp1292Tyr)
14g.23419275C>GCA389041753MYH7c.3874G>C (p.Asp1292His)
14g.23419275C>TCA389041754MYH7c.3874G>A (p.Asp1292Asn)
14g.23419276C>ACA485620159MYH7c.3873G>T (p.Leu1291=)
14g.23419276C=CA2123444573MYH7c.3873G= (p.Leu1291=)
14g.23419276C>GCA485620156MYH7c.3873G>C (p.Leu1291=)
14g.23419276C>TCA257814681MYH7c.3873G>A (p.Leu1291=)
dbSNP
14g.23419277A>CCA389041757MYH7c.3872T>G (p.Leu1291Arg)
14g.23419277A>GCA389041758MYH7c.3872T>C (p.Leu1291Pro)
14g.23419277A>TCA389041759MYH7c.3872T>A (p.Leu1291Gln)
14g.23419278G>ACA485620164MYH7c.3871C>T (p.Leu1291=)
14g.23419278G>CCA389041760MYH7c.3871C>G (p.Leu1291Val)
14g.23419278G>TCA389041762MYH7c.3871C>A (p.Leu1291Met)
14g.23419279C>ACA389041766MYH7c.3870G>T (p.Gln1290His)
14g.23419279C>GCA389041764MYH7c.3870G>C (p.Gln1290His)
14g.23419279C>TCA485620171MYH7c.3870G>A (p.Gln1290=)
14g.23419280T>ACA389041767MYH7c.3869A>T (p.Gln1290Leu)
COSMIC
14g.23419280T>CCA389041768MYH7c.3869A>G (p.Gln1290Arg)
14g.23419280T>GCA389041769MYH7c.3869A>C (p.Gln1290Pro)
14g.23419281G>ACA389041771MYH7c.3868C>T (p.Gln1290Ter)
14g.23419281G>CCA389041773MYH7c.3868C>G (p.Gln1290Glu)
14g.23419281G>TCA389041775MYH7c.3868C>A (p.Gln1290Lys)
14g.23419282C>ACA485620179MYH7c.3867G>T (p.Arg1289=)
14g.23419282C>GCA485620181MYH7c.3867G>C (p.Arg1289=)
14g.23419282C>TCA485620183MYH7c.3867G>A (p.Arg1289=)
14g.23419283C>ACA389041776MYH7c.3866G>T (p.Arg1289Leu)
14g.23419283C=CA2123444583MYH7c.3866G= (p.Arg1289=)
14g.23419283C>GCA389041777MYH7c.3866G>C (p.Arg1289Pro)
ClinVar
14g.23419283C>TCA389041779MYH7c.3866G>A (p.Arg1289Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419284G>ACA16043997MYH7c.3865C>T (p.Arg1289Trp)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419284G>CCA16614083MYH7c.3865C>G (p.Arg1289Gly)
ClinVar dbSNP
14g.23419284G=CA2123444598MYH7c.3865C= (p.Arg1289=)
14g.23419284G>TCA485620189MYH7c.3865C>A (p.Arg1289=)
14g.23419285G>ACA485620195MYH7c.3864C>T (p.Ser1288=)
14g.23419285G>CCA014192MYH7c.3864C>G (p.Ser1288=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419285G=CA2123444615MYH7c.3864C= (p.Ser1288=)
14g.23419285G>TCA485620198MYH7c.3864C>A (p.Ser1288=)
COSMIC
14g.23419286G>ACA389041785MYH7c.3863C>T (p.Ser1288Phe)
14g.23419286G>CCA389041786MYH7c.3863C>G (p.Ser1288Cys)
14g.23419286G>TCA389041783MYH7c.3863C>A (p.Ser1288Tyr)
gnomAD v4
14g.23419287A>CCA389041788MYH7c.3862T>G (p.Ser1288Ala)
14g.23419287A>GCA389041789MYH7c.3862T>C (p.Ser1288Pro)
14g.23419287A>TCA389041791MYH7c.3862T>A (p.Ser1288Thr)
14g.23419288C>ACA485620204MYH7c.3861G>T (p.Leu1287=)
14g.23419288C=CA2123444621MYH7c.3861G= (p.Leu1287=)
14g.23419288C>GCA014182MYH7c.3861G>C (p.Leu1287=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419288C>TCA485620208MYH7c.3861G>A (p.Leu1287=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419289A>CCA389041793MYH7c.3860T>G (p.Leu1287Arg)
14g.23419289A>GCA389041795MYH7c.3860T>C (p.Leu1287Pro)
14g.23419289A>TCA389041797MYH7c.3860T>A (p.Leu1287Gln)
14g.23419290G>ACA485620213MYH7c.3859C>T (p.Leu1287=)
14g.23419290G>CCA389041798MYH7c.3859C>G (p.Leu1287Val)
14g.23419290G>TCA389041800MYH7c.3859C>A (p.Leu1287Met)
14g.23419291C>ACA389041801MYH7c.3858G>T (p.Glu1286Asp)
dbSNP
14g.23419291C=CA2123444626MYH7c.3858G= (p.Glu1286=)
14g.23419291C>GCA389041802MYH7c.3858G>C (p.Glu1286Asp)
14g.23419291C>TCA485620219MYH7c.3858G>A (p.Glu1286=)
14g.23419292T>ACA389041806MYH7c.3857A>T (p.Glu1286Val)
14g.23419292T>CCA389041808MYH7c.3857A>G (p.Glu1286Gly)
14g.23419292T>GCA389041805MYH7c.3857A>C (p.Glu1286Ala)
14g.23419293C>ACA389041809MYH7c.3856G>T (p.Glu1286Ter)
14g.23419293C=CA2123444638MYH7c.3856G= (p.Glu1286=)
14g.23419293C>GCA389041810MYH7c.3856G>C (p.Glu1286Gln)
14g.23419293C>TCA014172MYH7c.3856G>A (p.Glu1286Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419294A>CCA485620231MYH7c.3855T>G (p.Gly1285=)
14g.23419294A>GCA485620233MYH7c.3855T>C (p.Gly1285=)
14g.23419294A>TCA485620235MYH7c.3855T>A (p.Gly1285=)
14g.23419295C>ACA389041813MYH7c.3854G>T (p.Gly1285Val)
14g.23419295C=CA2123444648MYH7c.3854G= (p.Gly1285=)
14g.23419295C>GCA389041814MYH7c.3854G>C (p.Gly1285Ala)
gnomAD v4
14g.23419295C>TCA389041816MYH7c.3854G>A (p.Gly1285Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419296dupCA2695219243MYH7c.3854dup
14g.23419296C>ACA389041817MYH7c.3854-1G>T (n.3854-1G>T)
ClinVar dbSNP
14g.23419296C=CA2123444655MYH7c.3854-1G= (n.3854-1G=)
14g.23419296C>GCA389041821MYH7c.3854-1G>C (n.3854-1G>C)
14g.23419296C>TCA389041819MYH7c.3854-1G>A (n.3854-1G>A)
ClinVar gnomAD v4
14g.23419297T>ACA257814714MYH7c.3854-2A>T (n.3854-2A>T)
dbSNP
14g.23419297T>CCA389041822MYH7c.3854-2A>G (n.3854-2A>G)
14g.23419297T>GCA389041824MYH7c.3854-2A>C (n.3854-2A>C)
14g.23419297T=CA2123444659MYH7c.3854-2A= (n.3854-2A=)
14g.23419298G>ACA613318035MYH7c.3854-3C>T (n.3854-3C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.23419298G>CCA257814716MYH7c.3854-3C>G (n.3854-3C>G)
dbSNP
14g.23419298G=CA2123444665MYH7c.3854-3C= (n.3854-3C=)
14g.23419298G>TCA257814717MYH7c.3854-3C>A (n.3854-3C>A)
dbSNP
14g.23419299G>CCA2123444672MYH7c.3854-4C>G (n.3854-4C>G)
dbSNP
14g.23419299G=CA2123444670MYH7c.3854-4C= (n.3854-4C=)
14g.23419300G>ACA039340MYH7c.3854-5C>T (n.3854-5C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419300G=CA2123444677MYH7c.3854-5C= (n.3854-5C=)
14g.23419301G>ACA2624229790MYH7c.3854-6C>T (n.3854-6C>T)
gnomAD v4
14g.23419305C=CA2123444683MYH7c.3854-10G= (n.3854-10G=)
14g.23419305C>TCA039270MYH7c.3854-10G>A (n.3854-10G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419306A=CA2123444692MYH7c.3854-11T= (n.3854-11T=)
14g.23419306A>GCA613318036MYH7c.3854-11T>C (n.3854-11T>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419307C>ACA2624229800MYH7c.3854-12G>T (n.3854-12G>T)
gnomAD v4
14g.23419307C>TCA2624229830MYH7c.3854-12G>A (n.3854-12G>A)
ClinVar gnomAD v4
14g.23419308C>ACA2624229833MYH7c.3854-13G>T (n.3854-13G>T)
gnomAD v4
14g.23419308C>TCA2624229836MYH7c.3854-13G>A (n.3854-13G>A)
gnomAD v4
14g.23419309A=CA2123444702MYH7c.3854-14T= (n.3854-14T=)
14g.23419309A>CCA039283MYH7c.3854-14T>G (n.3854-14T>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419309A>GCA2580088025MYH7c.3854-14T>C (n.3854-14T>C)
ClinVar
14g.23419310T>CCA2624229844MYH7c.3854-15A>G (n.3854-15A>G)
gnomAD v4
14g.23419313T>CCA2624229847MYH7c.3854-18A>G (n.3854-18A>G)
gnomAD v4
14g.23419314A>TCA2624229851MYH7c.3854-19T>A (n.3854-19T>A)
gnomAD v4
14g.23419315G>ACA2123444716MYH7c.3854-20C>T (n.3854-20C>T)
dbSNP
14g.23419315G>CCA2575504246MYH7c.3854-20C>G (n.3854-20C>G)
14g.23419315G=CA2123444712MYH7c.3854-20C= (n.3854-20C=)
14g.23419315G>TCA2624229857MYH7c.3854-20C>A (n.3854-20C>A)
gnomAD v4
14g.23419319A>CCA2624229860MYH7c.3854-24T>G (n.3854-24T>G)
gnomAD v4
14g.23419319A>TCA2624229883MYH7c.3854-24T>A (n.3854-24T>A)
gnomAD v4
14g.23419320G>TCA656016703MYH7c.3854-25C>A (n.3854-25C>A)
COSMIC
14g.23419322A>CCA2624229891MYH7c.3854-27T>G (n.3854-27T>G)
gnomAD v4
14g.23419323C=CA2123444717MYH7c.3854-28G= (n.3854-28G=)
14g.23419323C>GCA257814726MYH7c.3854-28G>C (n.3854-28G>C)
dbSNP gnomAD v4
14g.23419324T>CCA2123444724MYH7c.3854-29A>G (n.3854-29A>G)
dbSNP
14g.23419324T=CA2123444719MYH7c.3854-29A= (n.3854-29A=)
14g.23419326C>ACA2624229908MYH7c.3854-31G>T (n.3854-31G>T)
gnomAD v4
14g.23419326C=CA2123444729MYH7c.3854-31G= (n.3854-31G=)
14g.23419326C>GCA039288MYH7c.3854-31G>C (n.3854-31G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419326C>TCA257814728MYH7c.3854-31G>A (n.3854-31G>A)
dbSNP gnomAD v4
14g.23419327T>GCA2624229911MYH7c.3854-32A>C (n.3854-32A>C)
gnomAD v4
14g.23419328C=CA2123444733MYH7c.3854-33G= (n.3854-33G=)
14g.23419328C>GCA2624229915MYH7c.3854-33G>C (n.3854-33G>C)
gnomAD v4
14g.23419328C>TCA257814730MYH7c.3854-33G>A (n.3854-33G>A)
dbSNP gnomAD v4
14g.23419329T>CCA257814734MYH7c.3854-34A>G (n.3854-34A>G)
dbSNP
14g.23419329T=CA2123444737MYH7c.3854-34A= (n.3854-34A=)
14g.23419330C>ACA2624229917MYH7c.3854-35G>T (n.3854-35G>T)
gnomAD v4
14g.23419330C=CA2123444742MYH7c.3854-35G= (n.3854-35G=)
14g.23419330C>TCA2123444743MYH7c.3854-35G>A (n.3854-35G>A)
dbSNP
14g.23419331T>GCA2575504247MYH7c.3854-36A>C (n.3854-36A>C)
14g.23419332A=CA2123444746MYH7c.3854-37T= (n.3854-37T=)
14g.23419332A>GCA2123444748MYH7c.3854-37T>C (n.3854-37T>C)
dbSNP
14g.23419334C=CA2123444753MYH7c.3854-39G= (n.3854-39G=)
14g.23419334C>GCA613318037MYH7c.3854-39G>C (n.3854-39G>C)
dbSNP gnomAD v2 gnomAD v4
14g.23419335C=CA2123444761MYH7c.3854-40G= (n.3854-40G=)
14g.23419335C>GCA2123444762MYH7c.3854-40G>C (n.3854-40G>C)
dbSNP
14g.23419336C>ACA039299MYH7c.3854-41G>T (n.3854-41G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419336C=CA2123444764MYH7c.3854-41G= (n.3854-41G=)
14g.23419337C>ACA039315MYH7c.3854-42G>T (n.3854-42G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419337C=CA2123444769MYH7c.3854-42G= (n.3854-42G=)
14g.23419337C>TCA039310MYH7c.3854-42G>A (n.3854-42G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419340C=CA2123444777MYH7c.3854-45G= (n.3854-45G=)
14g.23419340C>TCA039323MYH7c.3854-45G>A (n.3854-45G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419341T>ACA2123444784MYH7c.3854-46A>T (n.3854-46A>T)
dbSNP gnomAD v4
14g.23419341T>CCA2123444785MYH7c.3854-46A>G (n.3854-46A>G)
dbSNP
14g.23419341T=CA2123444782MYH7c.3854-46A= (n.3854-46A=)
14g.23419342C>TCA2624229933MYH7c.3854-47G>A (n.3854-47G>A)
gnomAD v4
14g.23419345C=CA2123444788MYH7c.3854-50G= (n.3854-50G=)
14g.23419345C>TCA039334MYH7c.3854-50G>A (n.3854-50G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419346C>ACA2729046029MYH7c.3854-51G>T (n.3854-51G>T)
dbSNP
14g.23419346C>TCA2575504248MYH7c.3854-51G>A (n.3854-51G>A)
gnomAD v4
14g.23419348C=CA2123444795MYH7c.3854-53G= (n.3854-53G=)
14g.23419348C>GCA704287385MYH7c.3854-53G>C (n.3854-53G>C)
dbSNP gnomAD v4
14g.23419348C>TCA961071064MYH7c.3854-53G>A (n.3854-53G>A)
dbSNP gnomAD v3 gnomAD v4
14g.23419350A>GCA2575504249MYH7c.3854-55T>C (n.3854-55T>C)
14g.23419351G=CA2123444805MYH7c.3854-56C= (n.3854-56C=)
14g.23419351G>TCA2123444803MYH7c.3854-56C>A (n.3854-56C>A)
dbSNP
14g.23419352C>TCA2624229946MYH7c.3854-57G>A (n.3854-57G>A)
gnomAD v4
14g.23419353C>ACA2624229973MYH7c.3854-58G>T (n.3854-58G>T)
gnomAD v4
14g.23419353C>TCA2624229976MYH7c.3854-58G>A (n.3854-58G>A)
dbSNP gnomAD v4
14g.23419354C>ACA2624229979MYH7c.3854-59G>T (n.3854-59G>T)
gnomAD v4
14g.23419355T>CCA2624229982MYH7c.3854-60A>G (n.3854-60A>G)
gnomAD v4
14g.23419356C=CA2123444807MYH7c.3854-61G= (n.3854-61G=)
14g.23419356C>TCA2123444808MYH7c.3854-61G>A (n.3854-61G>A)
dbSNP
14g.23419357A>GCA2624229983MYH7c.3854-62T>C (n.3854-62T>C)
gnomAD v4
14g.23419358G>ACA2624229985MYH7c.3854-63C>T (n.3854-63C>T)
gnomAD v4

Number of alleles fetched