Variant #0000000185 (NC_000011.9:g.67257925G>A, NM_003977.2:c.784G>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.67257925G>A
Reference -
DB-ID AIP_000004
Frequency -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-27 12:08:22 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIP NM_003977.2 ?/? 5 c.784G>A r.(?) p.(Asp262Asn)