Variant #0000564401 (NC_000018.9:g.28681912C>A, NM_004949.3:c.23G>T (DSC2))

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.28681912C>A
DNA change (hg38) g.31101949C>A
Published as DSC2(NM_004949.3):c.23G>T (p.G8V), DSC2(NM_004949.5):c.23G>T (p.G8V)
ISCN -
DB-ID DSC2_000064 See all 4 reported entries
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) 8.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
DSC1 NM_004948.3 ?/. - c.*28773G>T r.(=) p.(=) -
DSC2 NM_004949.3 ?/. - c.23G>T r.(?) p.(Gly8Val) -


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