Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.155118752C>G | CA355128404 | MME | c.661C>G (p.Gln221Glu) n.504C>G | dbSNP gnomAD v2 gnomAD v4 |
3 | g.155118752C>T | CA10584006 | MME | c.661C>T (p.Gln221Ter) n.504C>T | ClinVar dbSNP gnomAD v4 |
3 | g.155118752C= | CA1412788811 | MME | c.661C= (p.Gln221=) n.504C= | dbSNP |