| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.132327369T>G | CA360808742 | MIR3936HG,SLC22A4 | c.917T>G (p.Ile306Arg) n.447T>G n.824+4820A>C c.389T>G (p.Ile130Arg) c.641T>G (p.Ile214Arg) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.132327369T>C | CA3403549 | MIR3936HG,SLC22A4 | c.917T>C (p.Ile306Thr) n.447T>C n.824+4820A>G c.389T>C (p.Ile130Thr) c.641T>C (p.Ile214Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.132327369T= | CA1583117644 | MIR3936HG,SLC22A4 | c.917T= (p.Ile306=) n.447T= n.824+4820A= c.389T= (p.Ile130=) c.641T= (p.Ile214=) | dbSNP |