Variant #0000001487 (NC_000006.12:g.32184665A>G, NM_001136.4:c.-443T>C (AGER))

Individual ID 00000313
Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32184665A>G
Published as −429T/C
Reference Foo Nian Wong et al. (2016), dbSNP
DB-ID AGER_000003 See all 6 reported entries
dbSNP ID rs1800625
Frequency 16/102
Variant remarks non-diabetic (ND-CKD)
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 2021-01-03 13:58:10 +08:00 (CST)
Date last edited 2021-09-01 10:55:21 +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.-443T>C - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000328 DNA PCRm;TaqMan AGER 10 Nuur Athirah Binti Mohd Daud