Variant #0000000591 (NC_000003.11:g.10183698C>G, NM_000551.4:c.167C>G (VHL))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.10183698C>G
Reference -
DB-ID VHL_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-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 2024-06-03 15:45:40 +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     
VHL NM_000551.3 ?/? - c.167C>G r.(?) p.(Ala56Gly)
VHL NM_000551.4 ?/? - c.167C>G r.(?) p.(Ala56Gly)