Variant #0000003337 (NC_000018.9:-, DSG2(NM_001943.3):c.473T>G)

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Families E and F had a

T>G change which replaces a valine with a glycine at

position 158 (V158G)
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID DSG2_00024 See all 2 reported entries
Frequency -
Variant remarks 473T>G
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSG2 NM_001943.3 ./. 05 c.473T>G - p.Val158Gly