Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.174198151T>C | CA15414718 | NSG2 | c.214-7049T>C (n.214-7049T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.174198151T>A | CA564831650 | NSG2 | c.214-7049T>A (n.214-7049T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.174198151T= | CA1602092060 | NSG2 | c.214-7049T= (n.214-7049T=) | dbSNP |