Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.56872885C>G | CA444212696 | MAP3K1 | c.1566C>G (p.Thr522=) c.1188C>G (p.Thr396=) c.1311C>G (p.Thr437=) c.1155C>G (p.Thr385=) c.1077C>G (p.Thr359=) n.1597C>G | dbSNP gnomAD v4 |
5 | g.56872885C>T | CA3272801 | MAP3K1 | c.1566C>T (p.Thr522=) c.1188C>T (p.Thr396=) c.1311C>T (p.Thr437=) c.1155C>T (p.Thr385=) c.1077C>T (p.Thr359=) n.1597C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |