Variant #0001123025 (NC_000011.9:g.71940824C>T, NC_000011.9(NM_001567.3):c.843+28C>T (INPPL1))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.71940824C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID INPPL1_000032
Frequency 1/12986
Freq. EA 0/8586
Freq. AA 1/4400
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 23:43:31 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
INPPL1 NM_001567.3 ?/? c.843+28C>T r.(=) p.(=)