Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.46601742T>C | CA14875743 | S100B | c.138+536A>G (n.138+536A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.46601742T>A | CA2392758189 | S100B | c.138+536A>T (n.138+536A>T) | dbSNP |
21 | g.46601742T>G | CA2392758190 | S100B | c.138+536A>C (n.138+536A>C) | dbSNP |