Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.7674246G>A | CA497717506 | TP53 | c.717C>T (p.Asn239=) c.321C>T (p.Asn107=) c.438C>T (p.Asn146=) c.696C>T (p.Asn232=) c.600C>T (p.Asn200=) c.240C>T (p.Asn80=) c.684C>T (p.Asn228=) | ClinVar dbSNP COSMIC |
17 | g.7674246G>T | CA397839156 | TP53 | c.717C>A (p.Asn239Lys) c.321C>A (p.Asn107Lys) c.438C>A (p.Asn146Lys) c.696C>A (p.Asn232Lys) c.600C>A (p.Asn200Lys) c.240C>A (p.Asn80Lys) c.684C>A (p.Asn228Lys) | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC |
17 | g.7674246G>C | CA16607851 | TP53 | c.717C>G (p.Asn239Lys) c.321C>G (p.Asn107Lys) c.438C>G (p.Asn146Lys) c.696C>G (p.Asn232Lys) c.600C>G (p.Asn200Lys) c.240C>G (p.Asn80Lys) c.684C>G (p.Asn228Lys) | ClinVar dbSNP COSMIC |