Variant #0001333996 (NC_000014.8:g.67147816T>C, NC_000014.8(NM_020806.4):c.65-9T>C (GPHN))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.67147816T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID GPHN_000011
Frequency 4085/13004
Freq. EA 1245/8598
Freq. AA 2840/4406
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 07:47:33 +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.65-9T>C r.(=) p.(=)