Variant #0000019311 (NC_000001.10:g.171208224C>A, NM_002021.1:c.-69C>A (FMO1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171208224C>A |
| DNA change (hg38) |
- |
| Published as |
-9536C>A |
| ISCN |
- |
| DB-ID |
FMO1_000009 See all 2 reported entries |
| Variant remarks |
variant in 5'UTR of non-coding exon 1, promoter P0 (not active in human liver, active in other species) Variant Error [EREF/EREFSEQ]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message. |
| Reference |
PubMed: Shephard 2007 |
| ClinVar ID |
- |
| dbSNP ID |
rs12720462 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Elizabeth A. Shephard |
| Database submission license |
No license selected |
| Created by |
Elizabeth A. Shephard |
| Date created |
2013-08-07 10:16:37 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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