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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGS NM_017541.2 +/. - c.30_31delinsAA - p.Phe10_Tyr11delinsLeuAsn


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