Variant #0000000091 (NC_000011.9:g.67257602C>T, NM_003977.2:c.562C>T (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.67257602C>T
Reference -
DB-ID AIP_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 3.0E-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 2020-03-03 13:47:17 +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 ?/? 4 c.562C>T r.(?) p.(Arg188Trp)