Variant #0000019555 (NC_000001.10:g.171059211C>T, NM_001002294.2:c.-918C>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.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 |
- |
| 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 15:46:48 +02:00 (CEST) |
| Date last edited |
2017-04-05 11:00:42 +02:00 (CEST) |

Variant on transcripts
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