Variant #0001717659 (NC_000019.9:g.10385743C>G, NC_000019.9(NM_000201.2):c.331+39C>G (ICAM1))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.10385743C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ICAM1_000023
Frequency 6402/12978
Freq. EA 3461/8584
Freq. AA 2941/4394
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 2013-05-05 23:05:18 +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.331+39C>G r.(=) p.(=)