Variant #0001123018 (NC_000011.9:g.71940633G>A, NC_000011.9(NM_001567.3):c.753+31G>A (INPPL1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.71940633G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID INPPL1_000051
Frequency 261/12986
Freq. EA 228/8586
Freq. AA 33/4400
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 2013-05-04 23:43:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
INPPL1 NM_001567.3 ?/? c.753+31G>A r.(=) p.(=)