Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.127852633G>A | CA13058842 | ENG | c.67+1656C>T (n.67+1656C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.127852633G>C | CA860211309 | ENG | c.67+1656C>G (n.67+1656C>G) | dbSNP |
9 | g.127852633G>T | CA860211307 | ENG | c.67+1656C>A (n.67+1656C>A) | dbSNP |