| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.84948545C>T | CA465896110 | NTRK2 | c.1764C>T (p.Ile588=) n.2334C>T n.2465C>T c.1800C>T (p.Ile600=) c.1848C>T (p.Ile616=) n.2878C>T n.2733C>T n.519C>T c.1332C>T (p.Ile444=) c.1380C>T (p.Ile460=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.84948545C>A | CA5105853 | NTRK2 | c.1764C>A (p.Ile588=) n.2334C>A n.2465C>A c.1800C>A (p.Ile600=) c.1848C>A (p.Ile616=) n.2878C>A n.2733C>A n.519C>A c.1332C>A (p.Ile444=) c.1380C>A (p.Ile460=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.84948545C>G | CA374009649 | NTRK2 | c.1764C>G (p.Ile588Met) n.2334C>G n.2465C>G c.1800C>G (p.Ile600Met) c.1848C>G (p.Ile616Met) n.2878C>G n.2733C>G n.519C>G c.1332C>G (p.Ile444Met) c.1380C>G (p.Ile460Met) | dbSNP gnomAD v4 |