Variant #0001566120 (NC_000017.10:g.18219570_18219571insCGT, NM_144775.2:c.467_468insCGT (SMCR8))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.18219570_18219571insCGT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SMCR8_000015
Frequency 1/12518
Freq. EA 1/8254
Freq. AA 0/4264
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 16:39:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SMCR8 NM_144775.2 ?/? c.467_468insCGT r.(?) p.(Ala156_Tyr157insVal)