Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.189868597G>ACA340599TP63c.1010G>A (p.Arg337Gln)
c.728G>A (p.Arg243Gln)
c.473G>A (p.Arg158Gln)
n.834G>A
c.959G>A (p.Arg320Gln)
c.1007G>A (p.Arg336Gln)
c.1004G>A (p.Arg335Gln)
c.971G>A (p.Arg324Gln)
ClinVar dbSNP COSMIC
3g.189868597G>CCA355755125TP63c.1010G>C (p.Arg337Pro)
c.728G>C (p.Arg243Pro)
c.473G>C (p.Arg158Pro)
n.834G>C
c.959G>C (p.Arg320Pro)
c.1007G>C (p.Arg336Pro)
c.1004G>C (p.Arg335Pro)
c.971G>C (p.Arg324Pro)
dbSNP

Number of alleles fetched