| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.6302617G>T | CA91798146 | WFS1 | c.*149G>T (n.*149G>T) c.2799G>T n.3007G>T | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.6302617G>A | CA10618112 | WFS1 | c.*149G>A (n.*149G>A) c.2799G>A n.3007G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.6302617G= | CA1435773022 | WFS1 | c.*149G= (n.*149G=) c.2799G= n.3007G= | dbSNP |