Variant #0001334055 (NC_000014.8:g.67555832_67555833insT, NC_000014.8(NM_020806.4):c.1237+40_1237+41insT (GPHN))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.67555832_67555833insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID GPHN_000070
Frequency 513/12310
Freq. EA 362/8144
Freq. AA 151/4166
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 16:41:19 +02:00 (CEST)
Date last edited 2013-05-05 07:47:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
GPHN NM_020806.4 ?/? c.1237+40_1237+41insT r.(=) p.(=)