| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.85270792G>A | CA118079 | BCL10 | c.172C>T (p.Arg58Ter) n.238C>T n.703C>T c.331C>T (p.Arg111Ter) c.118C>T (p.Arg40Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
| 1 | g.85270792G>C | CA118077 | BCL10 | c.172C>G (p.Arg58Gly) n.238C>G n.703C>G c.331C>G (p.Arg111Gly) c.118C>G (p.Arg40Gly) | ClinVar dbSNP |