Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47733844A>C | CA500652785 | TBX21 | c.390A>C (p.Gly130=) n.420A>C | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47733844A>T | CA8626260 | TBX21 | c.390A>T (p.Gly130=) n.420A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47733844A>G | CA8626259 | TBX21 | c.390A>G (p.Gly130=) n.420A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |