| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.132888141T>C | CA4883382 | TG | c.2334T>C (p.Pro778=) c.2073T>C (p.Pro691=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 8 | g.132888141T>A | CA463216650 | TG | c.2334T>A (p.Pro778=) c.2073T>A (p.Pro691=) | dbSNP gnomAD v3 gnomAD v4 |
| 8 | g.132888141T= | CA1820989945 | TG | c.2334T= (p.Pro778=) c.2073T= (p.Pro691=) | dbSNP |
| 8 | g.132888141T>G | CA463216651 | TG | c.2334T>G (p.Pro778=) c.2073T>G (p.Pro691=) | dbSNP gnomAD v4 |