| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.36575630C>T | CA122925 | RAG1,RAG2 | c.2326C>T (p.Arg776Trp) n.473G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.36575630C= | CA1964167703 | RAG1,RAG2 | c.2326C= (p.Arg776=) n.473G= | dbSNP |
| 11 | g.36575630C>A | CA474032427 | RAG1,RAG2 | c.2326C>A (p.Arg776=) n.473G>T | ClinVar dbSNP COSMIC |