Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.189866712G>TCA355754419TP63c.797G>T (p.Arg266Leu)
c.515G>T (p.Arg172Leu)
c.260G>T (p.Arg87Leu)
n.621G>T
c.746G>T (p.Arg249Leu)
c.794G>T (p.Arg265Leu)
c.791G>T (p.Arg264Leu)
c.758G>T (p.Arg253Leu)
ClinVar dbSNP
3g.189866712G>ACA118348TP63c.797G>A (p.Arg266Gln)
c.515G>A (p.Arg172Gln)
c.260G>A (p.Arg87Gln)
n.621G>A
c.746G>A (p.Arg249Gln)
c.794G>A (p.Arg265Gln)
c.791G>A (p.Arg264Gln)
c.758G>A (p.Arg253Gln)
ClinVar dbSNP COSMIC COSMIC COSMIC
3g.189866712G>CCA355754417TP63c.797G>C (p.Arg266Pro)
c.515G>C (p.Arg172Pro)
c.260G>C (p.Arg87Pro)
n.621G>C
c.746G>C (p.Arg249Pro)
c.794G>C (p.Arg265Pro)
c.791G>C (p.Arg264Pro)
c.758G>C (p.Arg253Pro)
ClinVar dbSNP

Number of alleles fetched