Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674247T>A | CA397839160 | TP53 | c.716A>T (p.Asn239Ile) c.320A>T (p.Asn107Ile) c.437A>T (p.Asn146Ile) c.695A>T (p.Asn232Ile) c.599A>T (p.Asn200Ile) c.239A>T (p.Asn80Ile) c.683A>T (p.Asn228Ile) | ClinVar dbSNP COSMIC |
17 | g.7674247T>G | CA16603055 | TP53 | c.716A>C (p.Asn239Thr) c.320A>C (p.Asn107Thr) c.437A>C (p.Asn146Thr) c.695A>C (p.Asn232Thr) c.599A>C (p.Asn200Thr) c.239A>C (p.Asn80Thr) c.683A>C (p.Asn228Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674247T>C | CA16603054 | TP53 | c.716A>G (p.Asn239Ser) c.320A>G (p.Asn107Ser) c.437A>G (p.Asn146Ser) c.695A>G (p.Asn232Ser) c.599A>G (p.Asn200Ser) c.239A>G (p.Asn80Ser) c.683A>G (p.Asn228Ser) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |