Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.6269344T>C | CA11634582 | WFS1 | c.4+7705T>C (n.4+7705T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.6269344T>G | CA1435753360 | WFS1 | c.4+7705T>G (n.4+7705T>G) | dbSNP |
4 | g.6269344T>A | CA1435753361 | WFS1 | c.4+7705T>A (n.4+7705T>A) | dbSNP |