| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.121538644T>A | CA5721071 | FGFR2 | c.696A>T (p.Val232=) n.351A>T c.351A>T (p.Val117=) n.3043A>T n.696A>T c.429A>T (p.Val143=) n.957A>T n.998A>T c.753A>T (p.Val251=) c.486A>T (p.Val162=) c.408A>T (p.Val136=) n.984A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.121538644T>C | CA5721070 | FGFR2 | c.696A>G (p.Val232=) n.351A>G c.351A>G (p.Val117=) n.3043A>G n.696A>G c.429A>G (p.Val143=) n.957A>G n.998A>G c.753A>G (p.Val251=) c.486A>G (p.Val162=) c.408A>G (p.Val136=) n.984A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.121538644T>G | CA471656483 | FGFR2 | c.696A>C (p.Val232=) n.351A>C c.351A>C (p.Val117=) n.3043A>C n.696A>C c.429A>C (p.Val143=) n.957A>C n.998A>C c.753A>C (p.Val251=) c.486A>C (p.Val162=) c.408A>C (p.Val136=) n.984A>C | dbSNP |