Variant #0000129884 (NC_000005.9:g.169535278G>A, NM_012188.4:c.800G>A (FOXI1))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.169535278G>A |
| DNA change (hg38) |
g.170108274G>A |
| Published as |
R267Q |
| ISCN |
- |
| DB-ID |
FOXI1_000003 See all 4 reported entries |
| Variant remarks |
FOX1 expression cloning and analysis in a promoter-reporter assay shows significantly decreased transcription of a SLC26A4 construct |
| Reference |
PubMed: Yang 2007, Journal: Yang 2007, OMIM:var0002 |
| ClinVar ID |
- |
| dbSNP ID |
rs121909341 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
7.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-09-09 15:53:59 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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