| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.49061382G>A | CA123707 | NTF4 | c.616C>T (p.Arg206Trp) c.243+373C>T (n.243+373C>T) c.646C>T (p.Arg216Trp) n.661C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 19 | g.49061382G= | CA2340217243 | NTF4 | c.616C= (p.Arg206=) c.243+373C= (n.243+373C=) c.646C= (p.Arg216=) n.661C= | dbSNP |