Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.61801834C>G | CA15677621 | FADS1,FADS2 | c.*577G>C (n.*577G>C) c.-55+8806C>G (n.-55+8806C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.61801834C>A | CA222951654 | FADS1,FADS2 | c.*577G>T (n.*577G>T) c.-55+8806C>A (n.-55+8806C>A) | dbSNP |