Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.114804160A>C | CA1874007092 | TNFSF15 | c.210+1643T>G (n.210+1643T>G) | dbSNP |
9 | g.114804160A>G | CA15597695 | TNFSF15 | c.210+1643T>C (n.210+1643T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.114804160A= | CA1874007090 | TNFSF15 | c.210+1643T= (n.210+1643T=) | dbSNP |