Variant #0000650407 (NC_000002.11:g.208992950G>A, CRYGC(NM_020989.3):c.502C>T)

Individual ID 00292550
Chromosome 2
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.208992950G>A
DNA change (hg38) g.208128226G>A
Published as -
ISCN -
DB-ID CRYGC_000003 See all 4 reported entries
Variant remarks 62 heterozygous, no homozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs28931604
Origin Germline
Segregation -
Frequency 62/2794 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00162 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYGC NM_020989.3 ?/. - c.502C>T r.(?) p.(Arg168Trp)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000293718 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq