Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.41961326C>T | CA10629179 | GLI3 | c.*3004G>A (n.*3004G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.41961326C>A | CA573767831 | GLI3 | c.*3004G>T (n.*3004G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.41961326C= | CA1702658722 | GLI3 | c.*3004G= (n.*3004G=) | dbSNP |