Variant #0000019559 (NC_000001.10:g.171059701A>G, NM_001002294.2:c.-428A>G (FMO3))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171059701A>G |
DNA change (hg38) |
g.171090560A>G |
Published as |
-2099A>G |
ISCN |
- |
DB-ID |
FMO3_000100 |
Variant remarks |
effect unknown |
Reference |
PubMed: Koukouritaki et al. 2005 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
? |
Frequency |
0/1204 control chromosomes |
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 16:17:21 +02:00 (CEST) |
Date last edited |
2017-04-05 11:00:42 +02:00 (CEST) |

Variant on transcripts
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