Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674247T>ACA397839160TP53c.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
17g.7674247T>GCA16603055TP53c.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
17g.7674247T>CCA16603054TP53c.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

Number of alleles fetched