Variant #0001103768 (NC_000011.9:g.64051823C>T, NC_000011.9(NM_020155.3):c.-2174C>T (GPR137))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.64051823C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID GPR137_000002
Frequency 388/12994
Freq. EA 350/8592
Freq. AA 38/4402
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-04 23:05:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
GPR137 NM_020155.3 ?/? c.-2174C>T r.(=) p.(=)
BAD NM_032989.2 ?/? c.18G>A r.(=) p.(=)