Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23425284A>CCA485622619MYH7c.2421T>G (p.Arg807=)
n.2527T>G
14g.23425284A>GCA485622620MYH7c.2421T>C (p.Arg807=)
n.2527T>C
14g.23425284A>TCA485622621MYH7c.2421T>A (p.Arg807=)
n.2527T>A
gnomAD v4
14g.23425285C>ACA389048452MYH7c.2420G>T (p.Arg807Leu)
n.2526G>T
gnomAD v4
14g.23425285C=CA2123457248MYH7c.2420G= (p.Arg807=)
n.2526G=
14g.23425285C>GCA389048453MYH7c.2420G>C (p.Arg807Pro)
n.2526G>C
ClinVar dbSNP
14g.23425285C>TCA032556MYH7c.2420G>A (p.Arg807His)
n.2526G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23425286G>ACA389048454MYH7c.2419C>T (p.Arg807Cys)
n.2525C>T
gnomAD v4
14g.23425286G>CCA389048456MYH7c.2419C>G (p.Arg807Gly)
n.2525C>G
ClinVar dbSNP
14g.23425286G>TCA389048455MYH7c.2419C>A (p.Arg807Ser)
n.2525C>A
COSMIC
14g.23425287T>ACA389048457MYH7c.2418A>T (p.Glu806Asp)
n.2524A>T
dbSNP
14g.23425287T>CCA485622622MYH7c.2418A>G (p.Glu806=)
n.2524A>G
14g.23425287T>GCA389048458MYH7c.2418A>C (p.Glu806Asp)
n.2524A>C
14g.23425287T=CA2123457255MYH7c.2418A= (p.Glu806=)
n.2524A=
14g.23425288T>ACA389048459MYH7c.2417A>T (p.Glu806Val)
n.2523A>T
14g.23425288T>CCA389048460MYH7c.2417A>G (p.Glu806Gly)
n.2523A>G
ClinVar dbSNP
14g.23425288T>GCA389048461MYH7c.2417A>C (p.Glu806Ala)
n.2523A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23425288T=CA2123457257MYH7c.2417A= (p.Glu806=)
n.2523A=
14g.23425289C>ACA389048462MYH7c.2416G>T (p.Glu806Ter)
n.2522G>T
COSMIC
14g.23425289C=CA2123457265MYH7c.2416G= (p.Glu806=)
n.2522G=
14g.23425289C>GCA389048463MYH7c.2416G>C (p.Glu806Gln)
n.2522G>C
14g.23425289C>TCA012304MYH7c.2416G>A (p.Glu806Lys)
n.2522G>A
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.23425290C>ACA485622626MYH7c.2415G>T (p.Leu805=)
n.2521G>T
14g.23425290C>GCA485622627MYH7c.2415G>C (p.Leu805=)
n.2521G>C
14g.23425290C>TCA485622628MYH7c.2415G>A (p.Leu805=)
n.2521G>A
gnomAD v4
14g.23425291A=CA2123457300MYH7c.2414T= (p.Leu805=)
n.2520T=
14g.23425291A>CCA389048464MYH7c.2414T>G (p.Leu805Arg)
n.2520T>G
dbSNP
14g.23425291A>GCA389048465MYH7c.2414T>C (p.Leu805Pro)
n.2520T>C
14g.23425291A>TCA389048466MYH7c.2414T>A (p.Leu805Gln)
n.2520T>A
14g.23425292G>ACA485622629MYH7c.2413C>T (p.Leu805=)
n.2519C>T
14g.23425292G>CCA389048467MYH7c.2413C>G (p.Leu805Val)
n.2519C>G
14g.23425292G>TCA389048468MYH7c.2413C>A (p.Leu805Met)
n.2519C>A
14g.23425293C>ACA485622634MYH7c.2412G>T (p.Leu804=)
n.2518G>T
ClinVar dbSNP gnomAD v4
14g.23425293C>GCA485622632MYH7c.2412G>C (p.Leu804=)
n.2518G>C
14g.23425293C>TCA485622630MYH7c.2412G>A (p.Leu804=)
n.2518G>A
14g.23425293_23425294delinsCACA2123457304MYH7c.2411_2412delinsTG (p.Leu804=)
n.2517_2518delinsTG
14g.23425294delCA2123457309MYH7c.2411del (p.Leu804ArgfsTer10)
n.2517del
ClinVar dbSNP
14g.23425294A=CA2123457310MYH7c.2411T= (p.Leu804=)
n.2517T=
14g.23425294A>CCA389048469MYH7c.2411T>G (p.Leu804Arg)
n.2517T>G
14g.23425294A>GCA389048470MYH7c.2411T>C (p.Leu804Pro)
n.2517T>C
ClinVar dbSNP
14g.23425294A>TCA389048471MYH7c.2411T>A (p.Leu804Gln)
n.2517T>A
14g.23425295G>ACA485622635MYH7c.2410C>T (p.Leu804=)
n.2516C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23425295G>CCA389048472MYH7c.2410C>G (p.Leu804Val)
n.2516C>G
14g.23425295G=CA2123457316MYH7c.2410C= (p.Leu804=)
n.2516C=
14g.23425295G>TCA389048473MYH7c.2410C>A (p.Leu804Met)
n.2516C>A
14g.23425296C>ACA389048474MYH7c.2409G>T (p.Lys803Asn)
n.2515G>T
14g.23425296C>GCA389048475MYH7c.2409G>C (p.Lys803Asn)
n.2515G>C
14g.23425296C>TCA485622636MYH7c.2409G>A (p.Lys803=)
n.2515G>A
gnomAD v4
14g.23425297T>ACA389048476MYH7c.2408A>T (p.Lys803Met)
n.2514A>T
14g.23425297T>CCA389048477MYH7c.2408A>G (p.Lys803Arg)
n.2514A>G

Number of alleles fetched