Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.68296248G>A | CA347796 | PIK3R1 | c.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 |
5 | g.68296248G= | CA1553406604 | PIK3R1 | c.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 |