Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7673535C>GCA397835662TP53c.993G>C (p.Gln331His)
c.597G>C (p.Gln199His)
c.714G>C (p.Gln238His)
c.972G>C (p.Gln324His)
c.782+646G>C (n.782+646G>C)
c.53G>C
c.876G>C (p.Gln292His)
c.516G>C (p.Gln172His)
c.960G>C (p.Gln320His)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535C>TCA10590137TP53c.993G>A (p.Gln331=)
c.597G>A (p.Gln199=)
c.714G>A (p.Gln238=)
c.972G>A (p.Gln324=)
c.782+646G>A (n.782+646G>A)
c.53G>A
c.876G>A (p.Gln292=)
c.516G>A (p.Gln172=)
c.960G>A (p.Gln320=)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC
17g.7673535C>ACA287486501TP53c.993G>T (p.Gln331His)
c.597G>T (p.Gln199His)
c.714G>T (p.Gln238His)
c.972G>T (p.Gln324His)
c.782+646G>T (n.782+646G>T)
c.53G>T
c.876G>T (p.Gln292His)
c.516G>T (p.Gln172His)
c.960G>T (p.Gln320His)
dbSNP COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched