| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.114796423C>T | CA15615238 | TNFSF15 | c.211-2855G>A (n.211-2855G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.114796423C>G | CA1874001344 | TNFSF15 | c.211-2855G>C (n.211-2855G>C) | ClinVar dbSNP |
| 9 | g.114796423C= | CA1874001343 | TNFSF15 | c.211-2855G= (n.211-2855G=) | dbSNP |