Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.16940375_16940376delinsTT | CA117394 | TNFRSF13B | c.581_582delinsAA (p.Ser194Ter) n.687_688delinsAA c.446-7200_446-7199delinsAA (n.446-7200_446-7199delinsAA) n.350-7439_350-7438delinsAA c.443_444delinsAA (p.Ser148Ter) | ClinVar dbSNP |
17 | g.16940375_16940376delinsCC | CA288282921 | TNFRSF13B | c.581_582delinsGG (p.Ser194Trp) n.687_688delinsGG c.446-7200_446-7199delinsGG (n.446-7200_446-7199delinsGG) n.350-7439_350-7438delinsGG c.443_444delinsGG (p.Ser148Trp) | dbSNP |