Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675161G>CCA16603058TP53c.451C>G (p.Pro151Ala)
c.55C>G (p.Pro19Ala)
c.172C>G (p.Pro58Ala)
c.430C>G (p.Pro144Ala)
n.707C>G
c.334C>G (p.Pro112Ala)
c.-27C>G (n.-27C>G)
c.418C>G (p.Pro140Ala)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675161G>TCA000198TP53c.451C>A (p.Pro151Thr)
c.55C>A (p.Pro19Thr)
c.172C>A (p.Pro58Thr)
c.430C>A (p.Pro144Thr)
n.707C>A
c.334C>A (p.Pro112Thr)
c.-27C>A (n.-27C>A)
c.418C>A (p.Pro140Thr)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675161G>ACA000200TP53c.451C>T (p.Pro151Ser)
c.55C>T (p.Pro19Ser)
c.172C>T (p.Pro58Ser)
c.430C>T (p.Pro144Ser)
n.707C>T
c.334C>T (p.Pro112Ser)
c.-27C>T (n.-27C>T)
c.418C>T (p.Pro140Ser)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched