Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.109784115G>A | CA7046460 | IRS2 | c.1939C>T (p.Leu647=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.109784115G>C | CA119946 | IRS2 | c.1939C>G (p.Leu647Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.109784115G= | CA2118540345 | IRS2 | c.1939C= (p.Leu647=) | dbSNP |