Variant #0001997461 (NC_000023.10:g.153996899G>C, NC_000023.10(NM_001363.3):c.771+192G>C (DKC1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.153996899G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID DKC1_000004
Frequency 9/4525
Freq. EA 0/3107
Freq. AA 9/1418
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 16:50:35 +02:00 (CEST)
Date last edited 2013-05-06 10:29:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
DKC1 NM_001363.3 ?/? c.771+192G>C r.(=) p.(=)
SNORA36A NR_002969.1 ?/? n.97G>C r.(?) -
MIR644B NR_049842.1 ?/? n.29G>C r.(?) -