Variant #0001717642 (NC_000019.9:g.10381878G>C, NM_000201.2:c.43G>C (ICAM1))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.10381878G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ICAM1_000006
Frequency 1/12992
Freq. EA 1/8590
Freq. AA 0/4402
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 16:45:39 +02:00 (CEST)
Date last edited 2016-10-09 16:23:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ICAM1 NM_000201.2 ?/? c.43G>C r.(?) p.(Val15Leu)