Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674211A>C | CA000396 | TP53 | c.752T>G (p.Ile251Ser) c.356T>G (p.Ile119Ser) c.473T>G (p.Ile158Ser) c.731T>G (p.Ile244Ser) c.635T>G (p.Ile212Ser) c.275T>G (p.Ile92Ser) c.719T>G (p.Ile240Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 COSMIC |
17 | g.7674211A>G | CA397838899 | TP53 | c.752T>C (p.Ile251Thr) c.356T>C (p.Ile119Thr) c.473T>C (p.Ile158Thr) c.731T>C (p.Ile244Thr) c.635T>C (p.Ile212Thr) c.275T>C (p.Ile92Thr) c.719T>C (p.Ile240Thr) | ClinVar dbSNP |
17 | g.7674211A>T | CA397838901 | TP53 | c.752T>A (p.Ile251Asn) c.356T>A (p.Ile119Asn) c.473T>A (p.Ile158Asn) c.731T>A (p.Ile244Asn) c.635T>A (p.Ile212Asn) c.275T>A (p.Ile92Asn) c.719T>A (p.Ile240Asn) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC |