Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.156778698G>T | CA16042552 | ARID1B | c.1018G>T (p.Gly340Ter) c.769G>T (p.Gly257Ter) c.758G>T n.852G>T | ClinVar dbSNP gnomAD v4 |
6 | g.156778698G= | CA1675343676 | ARID1B | c.1018G= (p.Gly340=) c.769G= (p.Gly257=) c.758G= n.852G= | dbSNP |