Variant #0000167075 (NC_000001.10:g.171080089A>G, NM_001002294.2:c.778A>G (FMO3))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171080089A>G |
| DNA change (hg38) |
g.171110948A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FMO3_000031 See all 3 reported entries |
| Variant remarks |
expected to affect N-oxygenation and S-oxygenation of drug substrates of FMO3 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-03-02 14:30:48 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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