Variant #0000001619 (NC_000006.12:g.32184610A>T, NM_001136.4:c.-388T>A (AGER))

Individual ID 00000350
Chromosome 6
Allele Unknown
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 56/171
Variant remarks DNR (diabetic non-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
Date created 2021-01-13 15:51:52 +08:00 (CST)
Date last edited 2021-09-08 14:54:34 +08:00 (CST)
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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