Variant #0000019554 (NC_000001.10:g.171059150C>G, NM_001002294.2:c.-979C>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.171059150C>G |
DNA change (hg38) |
g.171090009C>G |
Published as |
-2650C>G |
ISCN |
- |
DB-ID |
FMO3_000095 |
Variant remarks |
no effect on transcription in vitro |
Reference |
PubMed: Koukouritaki et al. 2005 |
ClinVar ID |
- |
dbSNP ID |
rs1736560 |
Origin |
Germline |
Segregation |
? |
Frequency |
HapMap 0.332 (Eur), 0.558 (Jpn), 0.124 (Afr) |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Ian Phillips |
Database submission license |
No license selected |
Created by |
Ian Phillips |
Date created |
2013-08-14 15:22:12 +02:00 (CEST) |
Date last edited |
2017-04-05 11:00:42 +02:00 (CEST) |

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