Variant #0000000291 (NC_000018.9:g.29101113G>A, NM_001943.3:c.430G>A (DSG2))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.29101113G>A
Reference -
DB-ID DSG2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 5.0E-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 2023-06-29 13:13:23 +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     
DSG2 NM_001943.3 ?/? - c.430G>A r.(?) p.(Glu144Lys)