Variant #0000000292 (NC_000018.9:g.29116266G>A, NM_001943.3:c.1525G>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.29116266G>A
Reference -
DB-ID DSG2_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 4.0E-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 13:13:44 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSG2 NM_001943.3 ?/? - c.1525G>A r.(?) p.(Asp509Asn)