Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673776G>A | CA000454 | TP53 | c.844C>T (p.Arg282Trp) c.448C>T (p.Arg150Trp) c.565C>T (p.Arg189Trp) c.823C>T (p.Arg275Trp) c.782+405C>T (n.782+405C>T) c.727C>T (p.Arg243Trp) c.367C>T (p.Arg123Trp) c.811C>T (p.Arg271Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
17 | g.7673776G>T | CA497715987 | TP53 | c.844C>A (p.Arg282=) c.448C>A (p.Arg150=) c.565C>A (p.Arg189=) c.823C>A (p.Arg275=) c.782+405C>A (n.782+405C>A) c.727C>A (p.Arg243=) c.367C>A (p.Arg123=) c.811C>A (p.Arg271=) | ClinVar dbSNP gnomAD v4 COSMIC |
17 | g.7673776G>C | CA000453 | TP53 | c.844C>G (p.Arg282Gly) c.448C>G (p.Arg150Gly) c.565C>G (p.Arg189Gly) c.823C>G (p.Arg275Gly) c.782+405C>G (n.782+405C>G) c.727C>G (p.Arg243Gly) c.367C>G (p.Arg123Gly) c.811C>G (p.Arg271Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |