Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.101727085C>G | CA1868423132 | GRIN3A | c.699+10196G>C (n.699+10196G>C) n.786+10196G>C | dbSNP |
9 | g.101727085C>T | CA13088007 | GRIN3A | c.699+10196G>A (n.699+10196G>A) n.786+10196G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.101727085C>A | CA1127421820 | GRIN3A | c.699+10196G>T (n.699+10196G>T) n.786+10196G>T | dbSNP gnomAD v3 gnomAD v4 |