Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.85753046G>T | CA11851857 | ARHGAP24 | c.268+31074G>T (n.268+31074G>T) c.-18+31074G>T (n.-18+31074G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.85753046G= | CA1473827522 | ARHGAP24 | c.268+31074G= (n.268+31074G=) c.-18+31074G= (n.-18+31074G=) | dbSNP |