Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.7675200C>GCA000166TP53c.412G>C (p.Ala138Pro)
c.16G>C (p.Ala6Pro)
c.133G>C (p.Ala45Pro)
c.391G>C (p.Ala131Pro)
n.668G>C
c.295G>C (p.Ala99Pro)
c.-66G>C (n.-66G>C)
c.379G>C (p.Ala127Pro)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC
17g.7675200C>ACA397842708TP53c.412G>T (p.Ala138Ser)
c.16G>T (p.Ala6Ser)
c.133G>T (p.Ala45Ser)
c.391G>T (p.Ala131Ser)
n.668G>T
c.295G>T (p.Ala99Ser)
c.-66G>T (n.-66G>T)
c.379G>T (p.Ala127Ser)
dbSNP COSMIC
17g.7675200C>TCA397842713TP53c.412G>A (p.Ala138Thr)
c.16G>A (p.Ala6Thr)
c.133G>A (p.Ala45Thr)
c.391G>A (p.Ala131Thr)
n.668G>A
c.295G>A (p.Ala99Thr)
c.-66G>A (n.-66G>A)
c.379G>A (p.Ala127Thr)
ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC

Number of alleles fetched