| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.141973545C>T | CA369566064 | MGAM,OR9A4,TAS2R38 | c.-3+27548C>T (n.-3+27548C>T) c.145G>A (p.Ala49Thr) c.*25-12851C>T (n.*25-12851C>T) | dbSNP gnomAD v4 |
| 7 | g.141973545C>G | CA115855 | MGAM,OR9A4,TAS2R38 | c.-3+27548C>G (n.-3+27548C>G) c.145G>C (p.Ala49Pro) c.*25-12851C>G (n.*25-12851C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.141973545C>A | CA369566062 | MGAM,OR9A4,TAS2R38 | c.-3+27548C>A (n.-3+27548C>A) c.145G>T (p.Ala49Ser) c.*25-12851C>A (n.*25-12851C>A) | dbSNP gnomAD v4 |