Variant #0000849669 (NC_000008.10:g.90965965C>T, NC_000008.10(NM_002485.4):c.1398-46G>A (NBN))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.90965965C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NBN_000038
Frequency 9/12744
Freq. EA 0/8410
Freq. AA 9/4334
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 15:10:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NBN NM_002485.4 ?/? c.1398-46G>A r.(=) p.(=)