Variant #0000017090 (NC_000001.10:g.171076835A>G, NM_001002294.2:c.341A>G (FMO3))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171076835A>G |
| DNA change (hg38) |
g.171107694A>G |
| Published as |
g.15036A>G |
| ISCN |
- |
| DB-ID |
FMO3_000005 See all 3 reported entries |
| Variant remarks |
not causative of TMAU, no effect in vitro |
| Reference |
PubMed: Shimizu et al. 2007 |
| ClinVar ID |
- |
| dbSNP ID |
rs186763441 |
| Origin |
Germline |
| Segregation |
no |
| Frequency |
0/100 chromosomes |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00074 View details |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-02-19 22:30:03 +01:00 (CET) |
| Date last edited |
2017-04-05 15:03:22 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|