Variant #0000003397 (NC_000018.9:-, DSG2(NM_001943.3):c.167T>A)

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type A novel

mutation in DSG2, V56M, was detected in an individual

carrying the 2146-1GC mutation in
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID DSG2_00073
Frequency -
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSG2 NM_001943.3 ./. 03 c.167T>A - p.Val56Glu