Variant #0001916823 (NC_000022.10:g.30051642C>T, NM_000268.3:c.576C>T (NF2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.30051642C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NF2_000030
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 07:46:00 +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.576C>T r.(=) p.(=)