Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675076T>CCA16603027TP53c.536A>G (p.His179Arg)
c.140A>G (p.His47Arg)
c.257A>G (p.His86Arg)
c.515A>G (p.His172Arg)
n.792A>G
n.44A>G
c.419A>G (p.His140Arg)
c.59A>G (p.His20Arg)
c.503A>G (p.His168Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675076T>ACA16603029TP53c.536A>T (p.His179Leu)
c.140A>T (p.His47Leu)
c.257A>T (p.His86Leu)
c.515A>T (p.His172Leu)
n.792A>T
n.44A>T
c.419A>T (p.His140Leu)
c.59A>T (p.His20Leu)
c.503A>T (p.His168Leu)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675076T>GCA16603032TP53c.536A>C (p.His179Pro)
c.140A>C (p.His47Pro)
c.257A>C (p.His86Pro)
c.515A>C (p.His172Pro)
n.792A>C
n.44A>C
c.419A>C (p.His140Pro)
c.59A>C (p.His20Pro)
c.503A>C (p.His168Pro)
ClinVar dbSNP

Number of alleles fetched