| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.89227850C>T | CA277447 | TYR | c.1064C>T (p.Ala355Val) n.2717+43610G>A n.2732+43610G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.89227850C>A | CA382028292 | TYR | c.1064C>A (p.Ala355Glu) n.2717+43610G>T n.2732+43610G>T | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.89227850C>G | CA6221341 | TYR | c.1064C>G (p.Ala355Gly) n.2717+43610G>C n.2732+43610G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |