Variant #0000001622 (NC_000006.12:g.32184610A>T, AGER(NM_001136.4):c.-388T>A)

Individual ID 00000350
Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32184610A>T
Published as -374T/A
Reference Zhi Xiang Ng et al. (2012)
DB-ID AGER_000002 See all 6 reported entries
dbSNP ID rs886057791
Frequency 7/171
Variant remarks DR (diabetic retinopathy)
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
AGER NM_001136.4 +/. - c.-388T>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000364 DNA PCR;SEQ AGER 8 Nuur Athirah Binti Mohd Daud