Variant #0000944705 (NC_000003.11:g.186257377_186257378delinsTT, NM_017541.2:c.30_31delinsAA (CRYGS))
| Chromosome |
3 |
| 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.186257377_186257378delinsTT |
| DNA change (hg38) |
g.186539588_186539589delinsTT |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CRYGS_000016 See all 2 reported entries |
| Variant remarks |
functional analysis shows impaired tryptophan microenvironment, weakening stability under thermal and chemical stress, resulting in self-aggregation, lens opacification, and cataract |
| Reference |
PubMed: Vendra 2023 |
| 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 |
2023-11-13 12:00:14 +01:00 (CET) |
| Date last edited |
2023-11-13 13:11:48 +01:00 (CET) |

Variant on transcripts
|