| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.25809753G>C | CA339114745 | SELENON | c.772G>C (p.Gly258Arg) c.841G>C (p.Gly281Arg) c.943G>C (p.Gly315Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 1 | g.25809753G>A | CA223589 | SELENON | c.772G>A (p.Gly258Ser) c.841G>A (p.Gly281Ser) c.943G>A (p.Gly315Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |