| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.48751247G>A | CA9557831 | FUT1 | c.35C>T (p.Ala12Val) c.404C>T (p.Ala135Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.48751247G>T | CA406705282 | FUT1 | c.35C>A (p.Ala12Asp) c.404C>A (p.Ala135Asp) | dbSNP |
| 19 | g.48751247G= | CA2340052997 | FUT1 | c.35C= (p.Ala12=) c.404C= (p.Ala135=) | dbSNP |
| 19 | g.48751247G>C | CA406705280 | FUT1 | c.35C>G (p.Ala12Gly) c.404C>G (p.Ala135Gly) | dbSNP |