Variant #0000117572 (NC_000010.10:g.103990535_103990551dup, NM_005029.3:c.640_656dup (PITX3))
| Chromosome |
10 |
| 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.103990535_103990551dup |
| DNA change (hg38) |
g.102230778_102230794dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PITX3_000002 See all 19 reported entries |
| Variant remarks |
IHC shows retained nuclear localization; pcDNA3.1 in vitro expression cloning in B3 cells shows decreased DNA-binding, luciferase assay in lens epithelial cells shows reduced (0.32) transactivation activity |
| Reference |
PubMed: Verdin 2014, Journal: Verdin 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-06-18 09:59:16 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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