Variant #0000167023 (NC_000001.10:g.171077252A>C, NM_001002294.2:c.517A>C (FMO3))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171077252A>C |
| DNA change (hg38) |
g.171108111A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FMO3_000102 See all 2 reported entries |
| Variant remarks |
impaired benzydamine N-oxygenation in compound het with P153L |
| Reference |
PubMed: Mayatepek 2004 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Elizabeth A. Shephard |
| Database submission license |
No license selected |
| Created by |
Elizabeth A. Shephard |
| Date created |
2013-08-15 13:20:54 +02:00 (CEST) |
| Date last edited |
2020-06-05 15:14:47 +02:00 (CEST) |

Variant on transcripts
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