| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.139618677C>T | CA213359 | KCNK9 | c.706G>A (p.Gly236Arg) n.530G>A c.454G>A (p.Gly152Arg) n.567G>A c.670G>A (p.Gly224Arg) n.770G>A c.376G>A (p.Gly126Arg) n.837G>A | ClinVar dbSNP COSMIC COSMIC |
| 8 | g.139618677C>G | CA16609476 | KCNK9 | c.706G>C (p.Gly236Arg) n.530G>C c.454G>C (p.Gly152Arg) n.567G>C c.670G>C (p.Gly224Arg) n.770G>C c.376G>C (p.Gly126Arg) n.837G>C | ClinVar dbSNP |
| 8 | g.139618677C= | CA1824270533 | KCNK9 | c.706G= (p.Gly236=) n.530G= c.454G= (p.Gly152=) n.567G= c.670G= (p.Gly224=) n.770G= c.376G= (p.Gly126=) n.837G= | dbSNP |