| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.75776919C>G | CA986349581 | H3-3B | c.*1676G>C (n.*1676G>C) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75776919C>A | CA2275677781 | H3-3B | c.*1676G>T (n.*1676G>T) | dbSNP |
| 17 | g.75776919C>T | CA14387365 | H3-3B | c.*1676G>A (n.*1676G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |