Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7674242A>TCA397839091TP53c.721T>A (p.Ser241Thr)
c.325T>A (p.Ser109Thr)
c.442T>A (p.Ser148Thr)
c.700T>A (p.Ser234Thr)
c.604T>A (p.Ser202Thr)
c.244T>A (p.Ser82Thr)
c.688T>A (p.Ser230Thr)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674242A>CCA16603080TP53c.721T>G (p.Ser241Ala)
c.325T>G (p.Ser109Ala)
c.442T>G (p.Ser148Ala)
c.700T>G (p.Ser234Ala)
c.604T>G (p.Ser202Ala)
c.244T>G (p.Ser82Ala)
c.688T>G (p.Ser230Ala)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7674242A>GCA16603079TP53c.721T>C (p.Ser241Pro)
c.325T>C (p.Ser109Pro)
c.442T>C (p.Ser148Pro)
c.700T>C (p.Ser234Pro)
c.604T>C (p.Ser202Pro)
c.244T>C (p.Ser82Pro)
c.688T>C (p.Ser230Pro)
ClinVar dbSNP gnomAD v2 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched