Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.108728378A>C | CA13922134 | MYO16 | c.441+795A>C (n.441+795A>C) c.507+795A>C (n.507+795A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.108728378A>T | CA960075714 | MYO16 | c.441+795A>T (n.441+795A>T) c.507+795A>T (n.507+795A>T) | dbSNP gnomAD v3 gnomAD v4 |