Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.78063343G>A | CA264048609 | NRXN3 | c.-704+1022G>A (n.-704+1022G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.78063343G>C | CA2148681237 | NRXN3 | c.-704+1022G>C (n.-704+1022G>C) | dbSNP |
14 | g.78063343G= | CA2148681236 | NRXN3 | c.-704+1022G= (n.-704+1022G=) | dbSNP |