Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.41043978T>A | CA14756932 | TOP1 | c.58+14523T>A (n.58+14523T>A) n.212+14523T>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.41043978T>C | CA2364199939 | TOP1 | c.58+14523T>C (n.58+14523T>C) n.212+14523T>C | dbSNP |
20 | g.41043978T>G | CA2364199940 | TOP1 | c.58+14523T>G (n.58+14523T>G) n.212+14523T>G | dbSNP |