| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.11752494C>T | CA130676 | GNAL | c.377-359C>T (n.377-359C>T) c.61C>T (p.Arg21Ter) | ClinVar dbSNP COSMIC |
| 18 | g.11752494C>G | CA401925765 | GNAL | c.377-359C>G (n.377-359C>G) c.61C>G (p.Arg21Gly) | dbSNP gnomAD v4 |
| 18 | g.11752494C= | CA2284923504 | GNAL | c.377-359C= (n.377-359C=) c.61C= (p.Arg21=) | dbSNP |