Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81699165A>G | CA842879483 | HGF | c.*3416T>C (n.*3416T>C) | dbSNP |
7 | g.81699165A>C | CA1103717933 | HGF | c.*3416T>G (n.*3416T>G) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81699165A>T | CA15489032 | HGF | c.*3416T>A (n.*3416T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |