Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673802C>GCA10580917TP53c.818G>C (p.Arg273Pro)
c.422G>C (p.Arg141Pro)
c.539G>C (p.Arg180Pro)
c.797G>C (p.Arg266Pro)
c.782+379G>C (n.782+379G>C)
c.701G>C (p.Arg234Pro)
c.341G>C (p.Arg114Pro)
c.785G>C (p.Arg262Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673802C>TCA000434TP53c.818G>A (p.Arg273His)
c.422G>A (p.Arg141His)
c.539G>A (p.Arg180His)
c.797G>A (p.Arg266His)
c.782+379G>A (n.782+379G>A)
c.701G>A (p.Arg234His)
c.341G>A (p.Arg114His)
c.785G>A (p.Arg262His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC
17g.7673802C>ACA001530TP53c.818G>T (p.Arg273Leu)
c.422G>T (p.Arg141Leu)
c.539G>T (p.Arg180Leu)
c.797G>T (p.Arg266Leu)
c.782+379G>T (n.782+379G>T)
c.701G>T (p.Arg234Leu)
c.341G>T (p.Arg114Leu)
c.785G>T (p.Arg262Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched