Variant #0001925898 (NC_000022.10:g.37873004_37873012del, NM_002405.3:c.569_577del (MFNG))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.37873004_37873012del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MFNG_000032
Frequency 2/12518
Freq. EA 2/8254
Freq. AA 0/4264
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 16:50:05 +02:00 (CEST)
Date last edited 2013-05-06 08:09:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MFNG NM_002405.3 ?/? c.569_577del r.(?) p.(Val190_Trp193delinsGly)