Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.51746963A>C | CA407121551 | FPR1 | c.32T>G (p.Ile11Ser) | dbSNP |
19 | g.51746963A>G | CA9616539 | FPR1 | c.32T>C (p.Ile11Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.51746963A>T | CA407121559 | FPR1 | c.32T>A (p.Ile11Asn) | dbSNP |
19 | g.51746963A= | CA2341531244 | FPR1 | c.32T= (p.Ile11=) | dbSNP |