Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.101427580A>G | CA114314 | ALDOB | c.442T>C (p.Trp148Arg) n.68-942T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.101427580A>C | CA196957398 | ALDOB | c.442T>G (p.Trp148Gly) n.68-942T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.101427580A= | CA1868280108 | ALDOB | c.442T= (p.Trp148=) n.68-942T= | dbSNP |