Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.1004897_1004898insTT | CA992471840 | GRIN3B | c.1396_1397insTT (p.Gly466ValfsTer?) n.146_147insTT c.-183_-182insTT (n.-183_-182insTT) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.1004897_1004898insC | CA9030402 | GRIN3B | c.1396_1397insC (p.Gly466AlafsTer17) n.146_147insC c.-183_-182insC (n.-183_-182insC) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.1004897_1004898insCGTT | CA9030401 | GRIN3B | c.1396_1397insCGTT (p.Gly466AlafsTer18) n.146_147insCGTT c.-183_-182insCGTT (n.-183_-182insCGTT) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |