Variant #0000564431 (NC_000018.9:g.28972253G>A, DSG4(NM_177986.3):c.955G>A)

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.28972253G>A
DNA change (hg38) g.31392290G>A
Published as DSG4(NM_001134453.2):c.955G>A (p.D319N)
ISCN -
DB-ID DSG4_000009
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00055 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSG4 NM_177986.3 ?/. - c.955G>A r.(?) p.(Asp319Asn)