| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.18138997C>A | CA362835519 | TPMT | c.460G>T (p.Ala154Ser) c.391G>T (p.Ala131Ser) | dbSNP gnomAD v4 |
| 6 | g.18138997C>T | CA122645 | TPMT | c.460G>A (p.Ala154Thr) c.391G>A (p.Ala131Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.18138997C>G | CA362835520 | TPMT | c.460G>C (p.Ala154Pro) c.391G>C (p.Ala131Pro) | dbSNP |
| 6 | g.18138997C= | CA891834522 | TPMT | c.460G= (p.Ala154=) c.391G= (p.Ala131=) | dbSNP |