Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.101427578C>T | CA16041285 | ALDOB | c.444G>A (p.Trp148Ter) n.68-940G>A | ClinVar dbSNP COSMIC |
9 | g.101427578C>G | CA374265347 | ALDOB | c.444G>C (p.Trp148Cys) n.68-940G>C | dbSNP gnomAD v4 |
9 | g.101427578C= | CA1868280107 | ALDOB | c.444G= (p.Trp148=) n.68-940G= | dbSNP |