Variant #0000002102 (NC_000006.12:g.32182039T>C, NC_000006.12(NM_001136.4):c.964+208A>G (AGER))

Individual ID 00000449
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.32182039T>C
Published as 2184A/G
Reference Z X Ng et al. (2012), dbSNP
DB-ID AGER_000005 See all 4 reported entries
dbSNP ID rs3134940
Frequency 73/98
Variant remarks -
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 2021-02-22 16:39:03 +08:00 (CST)
Date last edited 2021-09-05 14:45:54 +08:00 (CST)
Options




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.964+208A>G - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000487 DNA PCRdig AGER 6 Nuur Athirah Binti Mohd Daud