Variant #0001925934 (NC_000022.10:g.37876862C>T, NC_000022.10(NM_002405.3):c.256-55G>A (MFNG))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.37876862C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MFNG_000068
Frequency 10/4566
Freq. EA 10/3182
Freq. AA 0/1384
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 08:09:24 +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.256-55G>A r.(=) p.(=)