Variant #0001335618 (NC_000014.8:g.69262737C>T, NC_000014.8(NM_001244698.1):c.-3082G>A (ZFP36L1))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.69262737C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ZFP36L1_000028
Frequency 91/12280
Freq. EA 1/8098
Freq. AA 90/4182
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 07:51:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ZFP36L1 NM_001244698.1 ?/? c.-3082G>A r.(=) p.(=)