Variant #0000017143 (NC_000001.10:g.171061871G>T, FMO3(NM_001002294.2):c.72G>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.171061871G>T |
DNA change (hg38) |
g.171092730G>T |
Published as |
g.72G>T |
ISCN |
- |
DB-ID |
FMO3_000034 See all 2 reported entries |
Variant remarks |
- |
Reference |
PubMed: Koukouritaki et al. 2005, PubMed: Koukouritaki et al. 2007 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
no |
Frequency |
2/400 chromosomes (non-Latino white), 0/404 (Hispanic American), 0/402 (African American) |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Ornicha Prapapan |
Database submission license |
No license selected |
Created by |
Ornicha Prapapan |

Variant on transcripts
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