Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673800C>GCA16603092TP53c.820G>C (p.Val274Leu)
c.424G>C (p.Val142Leu)
c.541G>C (p.Val181Leu)
c.799G>C (p.Val267Leu)
c.782+381G>C (n.782+381G>C)
c.703G>C (p.Val235Leu)
c.343G>C (p.Val115Leu)
c.787G>C (p.Val263Leu)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673800C>TCA397836967TP53c.820G>A (p.Val274Ile)
c.424G>A (p.Val142Ile)
c.541G>A (p.Val181Ile)
c.799G>A (p.Val267Ile)
c.782+381G>A (n.782+381G>A)
c.703G>A (p.Val235Ile)
c.343G>A (p.Val115Ile)
c.787G>A (p.Val263Ile)
dbSNP COSMIC
17g.7673800C>ACA16603088TP53c.820G>T (p.Val274Phe)
c.424G>T (p.Val142Phe)
c.541G>T (p.Val181Phe)
c.799G>T (p.Val267Phe)
c.782+381G>T (n.782+381G>T)
c.703G>T (p.Val235Phe)
c.343G>T (p.Val115Phe)
c.787G>T (p.Val263Phe)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched