Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.97855197G>T | CA12994273 | FOXE1 | c.*161G>T (n.*161G>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.97855197G>A | CA1866643603 | FOXE1 | c.*161G>A (n.*161G>A) | dbSNP gnomAD v4 |
9 | g.97855197G>C | CA1866643604 | FOXE1 | c.*161G>C (n.*161G>C) | dbSNP gnomAD v4 |