Variant #0000000004 (NC_000011.9:g.67250676G>A, NM_003977.2:c.47G>A (AIP))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.67250676G>A
Reference -
DB-ID AIP_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00196 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 08:50:12 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIP NM_003977.2 ?/? 1 c.47G>A r.(?) p.(Arg16His)