| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.102230777G>A | CA16042675 | GBF1,PITX3 | c.646C>T (p.Gln216Ter) c.664C>T (p.Gln222Ter) c.-150G>A (n.-150G>A) c.-288G>A (n.-288G>A) | ClinVar dbSNP |
| 10 | g.102230777G= | CA1932539262 | GBF1,PITX3 | c.646C= (p.Gln216=) c.664C= (p.Gln222=) c.-150G= (n.-150G=) c.-288G= (n.-288G=) | dbSNP |