| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.133777188G>T | CA2625470 | TF | c.2012G>T (p.Gly671Val) c.743G>T n.3006G>T c.1880G>T (p.Gly627Val) c.1631G>T (p.Gly544Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.133777188G>A | CA122561 | TF | c.2012G>A (p.Gly671Glu) c.743G>A n.3006G>A c.1880G>A (p.Gly627Glu) c.1631G>A (p.Gly544Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |