Variant #0001774705 (NC_000019.9:g.43026225_43026226insGCCT, NM_001712.4:c.553_554insAGGC (CEACAM1))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.43026225_43026226insGCCT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CEACAM1_000065
Frequency 11/12516
Freq. EA 11/8252
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 01:29:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CEACAM1 NM_001712.4 ?/? c.553_554insAGGC r.(?) p.(Leu185Glnfs*26)