Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.156868201C>T | CA10584138 | NTRK1 | c.364C>T (p.Gln122Ter) c.526C>T (p.Gln176Ter) c.436C>T (p.Gln146Ter) n.313-5432C>T n.584C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.156868201C= | CA1200782095 | NTRK1 | c.364C= (p.Gln122=) c.526C= (p.Gln176=) c.436C= (p.Gln146=) n.313-5432C= n.584C= | dbSNP |