Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.55248613C>A | CA3863423 | HCRTR2 | c.224-26C>A (n.224-26C>A) c.29-26C>A (n.29-26C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55248613C>T | CA567639511 | HCRTR2 | c.224-26C>T (n.224-26C>T) c.29-26C>T (n.29-26C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.55248613C= | CA2581586443 | HCRTR2 | c.224-26C= (n.224-26C=) c.29-26C= (n.29-26C=) | dbSNP |