| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.154571682G>T | CA343929 | CHRNB2 | c.859G>T (p.Val287Leu) c.865G>T (p.Val289Leu) c.349G>T (p.Val117Leu) n.1111G>T | ClinVar dbSNP |
| 1 | g.154571682G>C | CA341463 | CHRNB2 | c.859G>C (p.Val287Leu) c.865G>C (p.Val289Leu) c.349G>C (p.Val117Leu) n.1111G>C | ClinVar dbSNP |
| 1 | g.154571682G>A | CA341464 | CHRNB2 | c.859G>A (p.Val287Met) c.865G>A (p.Val289Met) c.349G>A (p.Val117Met) n.1111G>A | ClinVar dbSNP |