Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.156880036C>G | CA342940308 | NTRK1 | c.1904C>G (p.Pro635Arg) c.*676C>G (n.*676C>G) c.2084C>G (p.Pro695Arg) c.52C>G c.2075C>G (p.Pro692Arg) c.2066C>G (p.Pro689Arg) c.1976C>G (p.Pro659Arg) n.2537C>G n.36C>G | dbSNP |
1 | g.156880036C>A | CA342940307 | NTRK1 | c.1904C>A (p.Pro635Gln) c.*676C>A (n.*676C>A) c.2084C>A (p.Pro695Gln) c.52C>A c.2075C>A (p.Pro692Gln) c.2066C>A (p.Pro689Gln) c.1976C>A (p.Pro659Gln) n.2537C>A n.36C>A | dbSNP |
1 | g.156880036C>T | CA256288 | NTRK1 | c.1904C>T (p.Pro635Leu) c.*676C>T (n.*676C>T) c.2084C>T (p.Pro695Leu) c.52C>T c.2075C>T (p.Pro692Leu) c.2066C>T (p.Pro689Leu) c.1976C>T (p.Pro659Leu) n.2537C>T n.36C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |