Variant #0000692566 (NC_000018.9:g.28681901C>A, NM_004949.3:c.34G>T (DSC2))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.28681901C>A
DNA change (hg38) -
Published as DSC2(NM_004949.3):c.34G>T (p.G12*)
ISCN -
DB-ID DSC2_000244 See all 2 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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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.*28784G>T r.(=) p.(=) -
DSC2 NM_004949.3 +?/. - c.34G>T r.(?) p.(Gly12Ter) -


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