Variant #0000019555 (NC_000001.10:g.171059211C>T, FMO3(NM_001002294.2):c.-918C>T)
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.171059211C>T |
DNA change (hg38) |
g.171090070C>T |
Published as |
-2589C>T |
ISCN |
- |
DB-ID |
FMO3_000096 |
Variant remarks |
no effect on transcription in vitro |
Reference |
PubMed: Koukouritaki et al. 2005 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
? |
Frequency |
0.040 (white American), 0.007 (African American), 0.007 (Hispanic American) |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Ian Phillips |
Database submission license |
No license selected |
Created by |
Ian Phillips |

Variant on transcripts
|
|