Variant #0001023282 (NC_000010.10:g.105048378C>T, NM_032727.3:c.1452C>T (INA))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.105048378C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID INA_000035
Frequency 1/13002
Freq. EA 0/8598
Freq. AA 1/4404
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 20:28:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
INA NM_032727.3 ?/? c.1452C>T r.(=) p.(=)