Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.69843305C>T | CA98891941 | SULT1E1 | c.772+856G>A (n.772+856G>A) c.270+856G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.69843305C>G | CA98891934 | SULT1E1 | c.772+856G>C (n.772+856G>C) c.270+856G>C | dbSNP gnomAD v3 gnomAD v4 |
4 | g.69843305C>A | CA98891930 | SULT1E1 | c.772+856G>T (n.772+856G>T) c.270+856G>T | dbSNP |