Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.4110564C>G | CA403391425 | MAP2K2 | n.834G>C c.395G>C (p.Gly132Ala) c.104G>C (p.Gly35Ala) n.592G>C | dbSNP |
19 | g.4110564C>T | CA250288 | MAP2K2 | n.834G>A c.395G>A (p.Gly132Asp) c.104G>A (p.Gly35Asp) n.592G>A | ClinVar dbSNP |
19 | g.4110564C>A | CA403391424 | MAP2K2 | n.834G>T c.395G>T (p.Gly132Val) c.104G>T (p.Gly35Val) n.592G>T | ClinVar dbSNP |