Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23422254_23422286delCA2580088204MYH7c.3145_3177del (p.Glu1049_Leu1059del)
n.3251_3283del
ClinVar
14g.23422276C>ACA389045374MYH7c.3149G>T (p.Arg1050Leu)
n.3255G>T
14g.23422276C=CA2123450804MYH7c.3149G= (p.Arg1050=)
n.3255G=
14g.23422276C>GCA035905MYH7c.3149G>C (p.Arg1050Pro)
n.3255G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23422276C>TCA389045372MYH7c.3149G>A (p.Arg1050Gln)
n.3255G>A
ClinVar dbSNP gnomAD v4
14g.23422277G>ACA013380MYH7c.3148C>T (p.Arg1050Ter)
n.3254C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23422277G>CCA389045375MYH7c.3148C>G (p.Arg1050Gly)
n.3254C>G
14g.23422277G=CA2123450812MYH7c.3148C= (p.Arg1050=)
n.3254C=
14g.23422277G>TCA035886MYH7c.3148C>A (p.Arg1050=)
n.3254C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23422278C>ACA389045377MYH7c.3147G>T (p.Glu1049Asp)
n.3253G>T
14g.23422278C=CA2123450820MYH7c.3147G= (p.Glu1049=)
n.3253G=
14g.23422278C>GCA389045378MYH7c.3147G>C (p.Glu1049Asp)
n.3253G>C
14g.23422278C>TCA485621901MYH7c.3147G>A (p.Glu1049=)
n.3253G>A
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23422279T>ACA389045380MYH7c.3146A>T (p.Glu1049Val)
n.3252A>T
14g.23422279T>CCA389045381MYH7c.3146A>G (p.Glu1049Gly)
n.3252A>G
14g.23422279T>GCA389045382MYH7c.3146A>C (p.Glu1049Ala)
n.3252A>C
14g.23422280C>ACA389045384MYH7c.3145G>T (p.Glu1049Ter)
n.3251G>T
14g.23422280C=CA2123450827MYH7c.3145G= (p.Glu1049=)
n.3251G=
14g.23422280C>GCA389045388MYH7c.3145G>C (p.Glu1049Gln)
n.3251G>C
14g.23422280C>TCA389045390MYH7c.3145G>A (p.Glu1049Lys)
n.3251G>A
dbSNP gnomAD v4
14g.23422281C>ACA485621909MYH7c.3144G>T (p.Leu1048=)
n.3250G>T
14g.23422281C=CA2123450832MYH7c.3144G= (p.Leu1048=)
n.3250G=
14g.23422281C>GCA485621910MYH7c.3144G>C (p.Leu1048=)
n.3250G>C
14g.23422281C>TCA035861MYH7c.3144G>A (p.Leu1048=)
n.3250G>A
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23422282A>CCA389045394MYH7c.3143T>G (p.Leu1048Arg)
n.3249T>G
14g.23422282A>GCA389045393MYH7c.3143T>C (p.Leu1048Pro)
n.3249T>C
14g.23422282A>TCA389045392MYH7c.3143T>A (p.Leu1048Gln)
n.3249T>A
14g.23422283G>ACA485621918MYH7c.3142C>T (p.Leu1048=)
n.3248C>T
14g.23422283G>CCA389045396MYH7c.3142C>G (p.Leu1048Val)
n.3248C>G
14g.23422283G>TCA389045398MYH7c.3142C>A (p.Leu1048Met)
n.3248C>A
COSMIC
14g.23422284G>ACA485621923MYH7c.3141C>T (p.Asp1047=)
n.3247C>T
ClinVar dbSNP
14g.23422284G>CCA389045399MYH7c.3141C>G (p.Asp1047Glu)
n.3247C>G
14g.23422284G=CA2123450843MYH7c.3141C= (p.Asp1047=)
n.3247C=
14g.23422284G>TCA389045400MYH7c.3141C>A (p.Asp1047Glu)
n.3247C>A
14g.23422285T>ACA389045402MYH7c.3140A>T (p.Asp1047Val)
n.3246A>T
14g.23422285T>CCA389045404MYH7c.3140A>G (p.Asp1047Gly)
n.3246A>G
14g.23422285T>GCA389045405MYH7c.3140A>C (p.Asp1047Ala)
n.3246A>C
14g.23422286C>ACA389045407MYH7c.3139G>T (p.Asp1047Tyr)
n.3245G>T
14g.23422286C>GCA389045408MYH7c.3139G>C (p.Asp1047His)
n.3245G>C
ClinVar gnomAD v4
14g.23422286C>TCA389045410MYH7c.3139G>A (p.Asp1047Asn)
n.3245G>A
COSMIC
14g.23422287C>ACA389045412MYH7c.3138G>T (p.Met1046Ile)
n.3244G>T
COSMIC
14g.23422287C=CA2123450857MYH7c.3138G= (p.Met1046=)
n.3244G=
14g.23422287C>GCA389045413MYH7c.3138G>C (p.Met1046Ile)
n.3244G>C
14g.23422287C>TCA035844MYH7c.3138G>A (p.Met1046Ile)
n.3244G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23422288A=CA2123450880MYH7c.3137T= (p.Met1046=)
n.3243T=
14g.23422288A>CCA035837MYH7c.3137T>G (p.Met1046Arg)
n.3243T>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23422288A>GCA389045415MYH7c.3137T>C (p.Met1046Thr)
n.3243T>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23422288A>TCA389045417MYH7c.3137T>A (p.Met1046Lys)
n.3243T>A
14g.23422289T>ACA389045422MYH7c.3136A>T (p.Met1046Leu)
n.3242A>T
14g.23422289T>CCA389045419MYH7c.3136A>G (p.Met1046Val)
n.3242A>G
ClinVar dbSNP gnomAD v4

Number of alleles fetched