| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.3121122C>A | CA403312356 | GNA11 | c.1023C>A (p.Phe341Leu) n.542C>A c.569C>A n.2344C>A | dbSNP |
| 19 | g.3121122C>T | CA9075124 | GNA11 | c.1023C>T (p.Phe341=) n.542C>T c.569C>T n.2344C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.3121122C>G | CA144606 | GNA11 | c.1023C>G (p.Phe341Leu) n.542C>G c.569C>G n.2344C>G | ClinVar dbSNP |
| 19 | g.3121122C= | CA2318685351 | GNA11 | c.1023C= (p.Phe341=) n.542C= c.569C= n.2344C= | dbSNP |