Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.68296248G>ACA347796PIK3R1c.992G>A (p.Arg331Gln)
c.1082G>A (p.Arg361Gln)
c.1892G>A (p.Arg631Gln)
c.*862G>A (n.*862G>A)
c.1817G>A (p.Arg606Gln)
c.1367G>A (p.Arg456Gln)
c.1916G>A (p.Arg639Gln)
c.1106G>A (p.Arg369Gln)
n.1557G>A
c.*858G>A (n.*858G>A)
c.929G>A (p.Arg310Gln)
c.899G>A (p.Arg300Gln)
c.803G>A (p.Arg268Gln)
c.875G>A (p.Arg292Gln)
c.584G>A (p.Arg195Gln)
c.488G>A (p.Arg163Gln)
n.2435G>A
c.1565G>A (p.Arg522Gln)
c.1619G>A (p.Arg540Gln)
ClinVar dbSNP
5g.68296248G=CA1553406604PIK3R1c.992G= (p.Arg331=)
c.1082G= (p.Arg361=)
c.1892G= (p.Arg631=)
c.*862G= (n.*862G=)
c.1817G= (p.Arg606=)
c.1367G= (p.Arg456=)
c.1916G= (p.Arg639=)
c.1106G= (p.Arg369=)
n.1557G=
c.*858G= (n.*858G=)
c.929G= (p.Arg310=)
c.899G= (p.Arg300=)
c.803G= (p.Arg268=)
c.875G= (p.Arg292=)
c.584G= (p.Arg195=)
c.488G= (p.Arg163=)
n.2435G=
c.1565G= (p.Arg522=)
c.1619G= (p.Arg540=)
dbSNP

Number of alleles fetched