| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.114406753A>G | CA136898 | WHRN | c.182T>C (p.Met61Thr) c.1838T>C (p.Met613Thr) n.2562T>C c.811T>C n.1719T>C c.689T>C (p.Met230Thr) c.785T>C (p.Met262Thr) c.1175T>C (p.Met392Thr) c.1871T>C (p.Met624Thr) c.1745T>C (p.Met582Thr) c.1628T>C (p.Met543Thr) c.548T>C (p.Met183Thr) n.2775T>C n.2673T>C n.2086T>C n.1984T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 9 | g.114406753A>T | CA374620810 | WHRN | c.182T>A (p.Met61Lys) c.1838T>A (p.Met613Lys) n.2562T>A c.811T>A n.1719T>A c.689T>A (p.Met230Lys) c.785T>A (p.Met262Lys) c.1175T>A (p.Met392Lys) c.1871T>A (p.Met624Lys) c.1745T>A (p.Met582Lys) c.1628T>A (p.Met543Lys) c.548T>A (p.Met183Lys) n.2775T>A n.2673T>A n.2086T>A n.1984T>A | dbSNP |