Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.68293310G>CCA16602527PIK3R1c.226G>C (p.Gly76Arg)
c.316G>C (p.Gly106Arg)
c.1126G>C (p.Gly376Arg)
c.*96G>C (n.*96G>C)
c.1051G>C (p.Gly351Arg)
c.601G>C (p.Gly201Arg)
n.767G>C
c.*92G>C (n.*92G>C)
c.163G>C (p.Gly55Arg)
c.133G>C (p.Gly45Arg)
c.37G>C (p.Gly13Arg)
c.109G>C (p.Gly37Arg)
c.1033G>C (p.Gly345Arg)
n.476G>C
n.1669G>C
c.145G>C (p.Gly49Arg)
n.525G>C
c.799G>C (p.Gly267Arg)
c.853G>C (p.Gly285Arg)
ClinVar dbSNP COSMIC COSMIC COSMIC
5g.68293310G>ACA16602526PIK3R1c.226G>A (p.Gly76Arg)
c.316G>A (p.Gly106Arg)
c.1126G>A (p.Gly376Arg)
c.*96G>A (n.*96G>A)
c.1051G>A (p.Gly351Arg)
c.601G>A (p.Gly201Arg)
n.767G>A
c.*92G>A (n.*92G>A)
c.163G>A (p.Gly55Arg)
c.133G>A (p.Gly45Arg)
c.37G>A (p.Gly13Arg)
c.109G>A (p.Gly37Arg)
c.1033G>A (p.Gly345Arg)
n.476G>A
n.1669G>A
c.145G>A (p.Gly49Arg)
n.525G>A
c.799G>A (p.Gly267Arg)
c.853G>A (p.Gly285Arg)
ClinVar dbSNP COSMIC COSMIC COSMIC

Number of alleles fetched