Variant #0000003362 (NC_000018.9:-, DSG2(NM_001943.3):c.166G>A)

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Yet, in the present study only the DSG2-V55M variant showed segregation with DCM in a family

pedi
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID DSG2_00022 See all 4 reported entries
Frequency -
Variant remarks c.209G>A
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.166G>A - p.Val56Met