Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.40071103dup | CA10603482 | BCOR | c.3108dup (p.Ala1037SerfsTer?) c.3054dup (p.Ala1019SerfsTer?) | ClinVar dbSNP |
X | g.40071103T= | CA2425443822 | BCOR | c.3108A= (p.Pro1036=) c.3054A= (p.Pro1018=) | dbSNP dbSNP |