Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674246G>ACA497717506TP53c.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
17g.7674246G>TCA397839156TP53c.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
17g.7674246G>CCA16607851TP53c.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

Number of alleles fetched