Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.61796827G>C | CA678985331 | FADS2,FEN1 | c.*323G>C (n.*323G>C) c.458-95G>C c.-55+3799G>C (n.-55+3799G>C) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.61796827G>T | CA15677620 | FADS2,FEN1 | c.*323G>T (n.*323G>T) c.458-95G>T c.-55+3799G>T (n.-55+3799G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |