Variant #0000863657 (NC_000008.10:g.126378991_126378993del, NC_000008.10(NM_173685.2):c.627-19_627-17del (NSMCE2))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.126378991_126378993del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NSMCE2_000046
Frequency 19/12518
Freq. EA 15/8254
Freq. AA 4/4264
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NSMCE2 NM_173685.2 ?/? c.627-19_627-17del r.(=) p.(=)