Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.30738552C>T | CA13808307 | ALOX5AP | c.70+2877C>T (n.70+2877C>T) c.241+2877C>T (n.241+2877C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.30738552C= | CA2082041481 | ALOX5AP | c.70+2877C= (n.70+2877C=) c.241+2877C= (n.241+2877C=) | dbSNP |