Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.36300203A>T | CA343275 | MYH9 | c.2963T>A (p.Val988Glu) n.3195T>A c.2900T>A (p.Val967Glu) | dbSNP |
22 | g.36300203A>G | CA411392103 | MYH9 | c.2963T>C (p.Val988Ala) n.3195T>C c.2900T>C (p.Val967Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
22 | g.36300203A>C | CA411392106 | MYH9 | c.2963T>G (p.Val988Gly) n.3195T>G c.2900T>G (p.Val967Gly) | dbSNP |