| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.81740948G>T | CA12513688 | HGF | c.865+2405C>A (n.865+2405C>A) c.850+2405C>A (n.850+2405C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.81740948G>C | CA1720893204 | HGF | c.865+2405C>G (n.865+2405C>G) c.850+2405C>G (n.850+2405C>G) | dbSNP |