| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.49115756C>A | CA16044219 | USP19 | c.1441G>T (p.Val481Leu) c.1615G>T (p.Val539Leu) c.1312G>T (p.Val438Leu) c.1660G>T (p.Val554Leu) c.1351G>T (p.Val451Leu) c.1504G>T (p.Val502Leu) c.1318G>T (p.Val440Leu) c.1471G>T (p.Val491Leu) c.1046G>T c.1654G>T (p.Val552Leu) c.1624G>T (p.Val542Leu) c.1666G>T (p.Val556Leu) c.1621G>T (p.Val541Leu) c.1363G>T (p.Val455Leu) c.1663G>T (p.Val555Leu) c.1612G>T (p.Val538Leu) c.1516G>T (p.Val506Leu) c.1609G>T (p.Val537Leu) c.1651G>T (p.Val551Leu) c.1657G>T (p.Val553Leu) c.1357G>T (p.Val453Leu) c.1510G>T (p.Val504Leu) c.1306G>T (p.Val436Leu) c.10G>T (p.Val4Leu) c.1618G>T (p.Val540Leu) c.1606G>T (p.Val536Leu) c.1585G>T (p.Val529Leu) | ClinVar dbSNP |
| 3 | g.49115756C>T | CA352752272 | USP19 | c.1441G>A (p.Val481Ile) c.1615G>A (p.Val539Ile) c.1312G>A (p.Val438Ile) c.1660G>A (p.Val554Ile) c.1351G>A (p.Val451Ile) c.1504G>A (p.Val502Ile) c.1318G>A (p.Val440Ile) c.1471G>A (p.Val491Ile) c.1046G>A c.1654G>A (p.Val552Ile) c.1624G>A (p.Val542Ile) c.1666G>A (p.Val556Ile) c.1621G>A (p.Val541Ile) c.1363G>A (p.Val455Ile) c.1663G>A (p.Val555Ile) c.1612G>A (p.Val538Ile) c.1516G>A (p.Val506Ile) c.1609G>A (p.Val537Ile) c.1651G>A (p.Val551Ile) c.1657G>A (p.Val553Ile) c.1357G>A (p.Val453Ile) c.1510G>A (p.Val504Ile) c.1306G>A (p.Val436Ile) c.10G>A (p.Val4Ile) c.1618G>A (p.Val540Ile) c.1606G>A (p.Val536Ile) c.1585G>A (p.Val529Ile) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |