Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.151572685G>ACA013518PRKAG2c.304C>T (p.His102Tyr)
c.1027C>T (p.His343Tyr)
c.1030C>T (p.His344Tyr)
c.307C>T (p.His103Tyr)
c.90C>T
n.373C>T
c.655C>T (p.His219Tyr)
n.524C>T
c.247C>T (p.His83Tyr)
n.1145C>T
c.*270C>T (n.*270C>T)
n.173C>T
c.*349C>T (n.*349C>T)
c.898C>T (p.His300Tyr)
c.798C>T (n.798C>T)
c.895C>T (p.His299Tyr)
n.763C>T
c.82C>T (p.His28Tyr)
n.376C>T
c.658C>T (p.His220Tyr)
c.*279C>T (n.*279C>T)
c.1018C>T (p.His340Tyr)
c.1015C>T (p.His339Tyr)
c.283C>T (p.His95Tyr)
ClinVar dbSNP
7g.151572685G=CA1752730170PRKAG2c.304C= (p.His102=)
c.1027C= (p.His343=)
c.1030C= (p.His344=)
c.307C= (p.His103=)
c.90C=
n.373C=
c.655C= (p.His219=)
n.524C=
c.247C= (p.His83=)
n.1145C=
c.*270C= (n.*270C=)
n.173C=
c.*349C= (n.*349C=)
c.898C= (p.His300=)
c.798C= (n.798C=)
c.895C= (p.His299=)
n.763C=
c.82C= (p.His28=)
n.376C=
c.658C= (p.His220=)
c.*279C= (n.*279C=)
c.1018C= (p.His340=)
c.1015C= (p.His339=)
c.283C= (p.His95=)
dbSNP
7g.151572685G>TCA370072144PRKAG2c.304C>A (p.His102Asn)
c.1027C>A (p.His343Asn)
c.1030C>A (p.His344Asn)
c.307C>A (p.His103Asn)
c.90C>A
n.373C>A
c.655C>A (p.His219Asn)
n.524C>A
c.247C>A (p.His83Asn)
n.1145C>A
c.*270C>A (n.*270C>A)
n.173C>A
c.*349C>A (n.*349C>A)
c.898C>A (p.His300Asn)
c.798C>A (n.798C>A)
c.895C>A (p.His299Asn)
n.763C>A
c.82C>A (p.His28Asn)
n.376C>A
c.658C>A (p.His220Asn)
c.*279C>A (n.*279C>A)
c.1018C>A (p.His340Asn)
c.1015C>A (p.His339Asn)
c.283C>A (p.His95Asn)
dbSNP gnomAD v4

Number of alleles fetched