| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.9764370G>T | CA16620319 | GRIN2A | c.3174C>A (p.His1058Gln) c.2703C>A (p.His901Gln) n.2767C>A c.*544C>A (n.*544C>A) c.2763C>A (p.His921Gln) n.2813C>A c.3015C>A (p.His1005Gln) c.2916C>A (p.His972Gln) c.3330C>A (p.His1110Gln) | ClinVar dbSNP |
| 16 | g.9764370G= | CA2206693202 | GRIN2A | c.3174C= (p.His1058=) c.2703C= (p.His901=) n.2767C= c.*544C= (n.*544C=) c.2763C= (p.His921=) n.2813C= c.3015C= (p.His1005=) c.2916C= (p.His972=) c.3330C= (p.His1110=) | dbSNP |