Variant #0001129485 (NC_000011.9:g.77553634G>T, NM_024684.2:c.92G>T (AAMDC))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.77553634G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAMDC_000006
Frequency 1/12984
Freq. EA 1/8584
Freq. AA 0/4400
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:37:25 +02:00 (CEST)
Date last edited 2018-09-30 11:53:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAMDC NM_024684.2 ?/? c.92G>T r.(?) p.(Gly31Val)