Variant #0001925950 (NC_000022.10:g.37882197G>C, NM_002405.3:c.19C>G (MFNG))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.37882197G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MFNG_000084
Frequency 8/12946
Freq. EA 8/8562
Freq. AA 0/4384
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 08:09:25 +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.19C>G r.(?) p.(Arg7Gly)