Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.151572685G>A | CA013518 | PRKAG2 | c.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 |
7 | g.151572685G= | CA1752730170 | PRKAG2 | c.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 |
7 | g.151572685G>T | CA370072144 | PRKAG2 | c.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 |