Variant #0000930938 (NC_000018.9:g.28649081C>T, NM_004949.3:c.2287G>A (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.28649081C>T
DNA change (hg38) -
Published as DSC2(NM_004949.5):c.2287G>A (p.A763T), DSC2(NM_024422.4):c.2287G>A (p.A763T)
ISCN -
DB-ID DSC2_000124 See all 3 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) 3.0E-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 2023-07-07 10:10:56 +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     
DSC2 NM_004949.3 ?/. - c.2287G>A r.(?) p.(Ala763Thr) -


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