Variant #0001140401 (NC_000011.9:g.105961382C>T, NM_015423.2:c.508C>T (AASDHPPT))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.105961382C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AASDHPPT_000031
Frequency 1/12996
Freq. EA 1/8594
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 16:37:25 +02:00 (CEST)
Date last edited 2018-09-30 11:46:47 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AASDHPPT NM_015423.2 ?/? c.508C>T r.(=) p.(=)