Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.88086259T>A | CA1989383025 | RAB38 | c.483+63416A>T (n.483+63416A>T) | dbSNP |
11 | g.88086259T>C | CA16424497 | RAB38 | c.483+63416A>G (n.483+63416A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.88086259T= | CA1989383023 | RAB38 | c.483+63416A= (n.483+63416A=) | dbSNP |