| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.50448593G>C | CA876049749 | DGKK | c.645+21441C>G (n.645+21441C>G) | dbSNP |
| X | g.50448593G>A | CA15007383 | DGKK | c.645+21441C>T (n.645+21441C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.50448593G= | CA2428872423 | DGKK | c.645+21441C= (n.645+21441C=) | dbSNP |