Variant #0000863636 (NC_000008.10:g.126194457T>G, NM_173685.2:c.377T>G (NSMCE2))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.126194457T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NSMCE2_000024
Frequency 37/12992
Freq. EA 0/8590
Freq. AA 37/4402
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 15:36:22 +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.377T>G r.(?) p.(Phe126Cys)