| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.52772131T>G | CA13220764 | MBL2 | c.-9-487A>C (n.-9-487A>C) c.-24-472A>C (n.-24-472A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.52772131T= | CA1910259653 | MBL2 | c.-9-487A= (n.-9-487A=) c.-24-472A= (n.-24-472A=) | dbSNP |