Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.120788801C>G | CA251420 | TSPAN12 | c.709G>C (p.Ala237Pro) c.688G>C (n.688G>C) c.634G>C (p.Ala212Pro) | ClinVar dbSNP |
7 | g.120788801C>T | CA369133754 | TSPAN12 | c.709G>A (p.Ala237Thr) c.688G>A (n.688G>A) c.634G>A (p.Ala212Thr) | dbSNP |