| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.114785492T>C | CA15600991 | TNFSF15 | c.*4960A>G (n.*4960A>G) c.5539A>G (n.5539A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.114785492T>A | CA858969428 | TNFSF15 | c.*4960A>T (n.*4960A>T) c.5539A>T (n.5539A>T) | dbSNP gnomAD v4 |