| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.799117C>G | CA2011681625 | WNK1 | c.760-14525C>G (n.760-14525C>G) | dbSNP |
| 12 | g.799117C>T | CA13761671 | WNK1 | c.760-14525C>T (n.760-14525C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.799117C= | CA2011681624 | WNK1 | c.760-14525C= (n.760-14525C=) | dbSNP |