| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.153704257T>A | CA358493432 | TLR2 | c.1350T>A (p.Ser450Arg) c.222-594T>A (n.222-594T>A) | dbSNP |
| 4 | g.153704257T>C | CA3110879 | TLR2 | c.1350T>C (p.Ser450=) c.222-594T>C (n.222-594T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.153704257T= | CA1504540801 | TLR2 | c.1350T= (p.Ser450=) c.222-594T= (n.222-594T=) | dbSNP |