Variant #0000167089 (NC_000001.10:g.171072965G>A, NM_001002294.2:c.172G>A (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.171072965G>A |
| DNA change (hg38) |
g.171103824G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FMO3_000007 See all 8 reported entries |
| Variant remarks |
expected to influence metabolism of drug (xenobiotic) substrates of FMO3 that undergo N-oxygenation |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00034 View details |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-02-28 23:18:48 +01:00 (CET) |
| Date last edited |
2017-04-05 15:09:25 +02:00 (CEST) |

Variant on transcripts
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