Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.114804733C>T | CA16372718 | TNFSF15 | c.210+1070G>A (n.210+1070G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.114804733C>G | CA1874007567 | TNFSF15 | c.210+1070G>C (n.210+1070G>C) | dbSNP |
9 | g.114804733C= | CA1874007566 | TNFSF15 | c.210+1070G= (n.210+1070G=) | dbSNP |