Variant #0001925893 (NC_000022.10:g.37872892C>A, NC_000022.10(NM_002405.3):c.647+42G>T (MFNG))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.37872892C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MFNG_000027
Frequency 1/13004
Freq. EA 1/8600
Freq. AA 0/4404
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 08:09:14 +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.647+42G>T r.(=) p.(=)