Variant #0000863648 (NC_000008.10:g.126369909T>C, NC_000008.10(NM_173685.2):c.520-45T>C (NSMCE2))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.126369909T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NSMCE2_000037
Frequency 147/13006
Freq. EA 1/8600
Freq. AA 146/4406
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 15:36:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NSMCE2 NM_173685.2 ?/? c.520-45T>C r.(=) p.(=)