| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.156876128G>C | CA342937952 | NTRK1 | c.1370G>C (p.Gly457Ala) c.*142G>C (n.*142G>C) c.1550G>C (p.Gly517Ala) c.1541G>C (p.Gly514Ala) c.1532G>C (p.Gly511Ala) c.1442G>C (p.Gly481Ala) n.2003G>C n.773G>C | dbSNP |
| 1 | g.156876128G>T | CA342937954 | NTRK1 | c.1370G>T (p.Gly457Val) c.*142G>T (n.*142G>T) c.1550G>T (p.Gly517Val) c.1541G>T (p.Gly514Val) c.1532G>T (p.Gly511Val) c.1442G>T (p.Gly481Val) n.2003G>T n.773G>T | dbSNP COSMIC COSMIC |
| 1 | g.156876128G>A | CA272998 | NTRK1 | c.1370G>A (p.Gly457Glu) c.*142G>A (n.*142G>A) c.1550G>A (p.Gly517Glu) c.1541G>A (p.Gly514Glu) c.1532G>A (p.Gly511Glu) c.1442G>A (p.Gly481Glu) n.2003G>A n.773G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |