Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.30737636C>A | CA247375832 | ALOX5AP | c.70+1961C>A (n.70+1961C>A) c.241+1961C>A (n.241+1961C>A) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.30737636C>T | CA2082040375 | ALOX5AP | c.70+1961C>T (n.70+1961C>T) c.241+1961C>T (n.241+1961C>T) | dbSNP |
13 | g.30737636C>G | CA13784452 | ALOX5AP | c.70+1961C>G (n.70+1961C>G) c.241+1961C>G (n.241+1961C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |