Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7673775C>A | CA000456 | TP53 | c.845G>T (p.Arg282Leu) c.449G>T (p.Arg150Leu) c.566G>T (p.Arg189Leu) c.824G>T (p.Arg275Leu) c.782+406G>T (n.782+406G>T) c.728G>T (p.Arg243Leu) c.368G>T (p.Arg123Leu) c.812G>T (p.Arg271Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
17 | g.7673775C>G | CA16603074 | TP53 | c.845G>C (p.Arg282Pro) c.449G>C (p.Arg150Pro) c.566G>C (p.Arg189Pro) c.824G>C (p.Arg275Pro) c.782+406G>C (n.782+406G>C) c.728G>C (p.Arg243Pro) c.368G>C (p.Arg123Pro) c.812G>C (p.Arg271Pro) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |
17 | g.7673775C>T | CA10575441 | TP53 | c.845G>A (p.Arg282Gln) c.449G>A (p.Arg150Gln) c.566G>A (p.Arg189Gln) c.824G>A (p.Arg275Gln) c.782+406G>A (n.782+406G>A) c.728G>A (p.Arg243Gln) c.368G>A (p.Arg123Gln) c.812G>A (p.Arg271Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |