Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.12050956G>C | CA13437480 | LINC02547 | n.57-7578G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.12050956G>T | CA1952643647 | LINC02547 | n.57-7578G>T | dbSNP |
11 | g.12050956G>A | CA1952643646 | LINC02547 | n.57-7578G>A | dbSNP |