Variant #0001916831 (NC_000022.10:g.30057159G>A, NC_000022.10(NM_000268.3):c.676-35G>A (NF2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.30057159G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NF2_000038
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
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 16:50:05 +02:00 (CEST)
Date last edited 2013-05-06 07:46:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NF2 NM_000268.3 ?/? c.676-35G>A r.(=) p.(=)