Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.58506844A>T | CA400363184 | MTMR4 | c.932T>A (p.Val311Glu) c.890T>A (p.Val297Glu) c.902T>A (p.Val301Glu) | dbSNP gnomAD v4 |
17 | g.58506844A>C | CA8674372 | MTMR4 | c.932T>G (p.Val311Gly) c.890T>G (p.Val297Gly) c.902T>G (p.Val301Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.58506844A>G | CA400363183 | MTMR4 | c.932T>C (p.Val311Ala) c.890T>C (p.Val297Ala) c.902T>C (p.Val301Ala) | dbSNP gnomAD v2 gnomAD v4 |