Variant #0000017143 (NC_000001.10:g.171061871G>T, NM_001002294.2:c.72G>T (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.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 |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Ornicha Prapapan |
| Database submission license |
No license selected |
| Created by |
Ornicha Prapapan |
| Date created |
2013-03-09 21:11:03 +01:00 (CET) |
| Date last edited |
2017-04-05 10:58:51 +02:00 (CEST) |

Variant on transcripts
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