Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.6269316A>C | CA1435753339 | WFS1 | c.4+7677A>C (n.4+7677A>C) | dbSNP |
4 | g.6269316A>T | CA11634581 | WFS1 | c.4+7677A>T (n.4+7677A>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.6269316A>G | CA1435753338 | WFS1 | c.4+7677A>G (n.4+7677A>G) | dbSNP |