Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.104279427A>T | CA378085611 | GSTO2 | c.424A>T (p.Asn142Tyr) c.340A>T (p.Asn114Tyr) c.366+1311A>T (n.366+1311A>T) n.275+1311A>T n.311A>T c.282+1311A>T (n.282+1311A>T) | dbSNP |
10 | g.104279427A>G | CA5681860 | GSTO2 | c.424A>G (p.Asn142Asp) c.340A>G (p.Asn114Asp) c.366+1311A>G (n.366+1311A>G) n.275+1311A>G n.311A>G c.282+1311A>G (n.282+1311A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |