Variant #0001015674 (NC_000018.9:g.28681875C>T, NM_004949.3:c.60G>A (DSC2))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.28681875C>T
DNA change (hg38) -
Published as DSC2(NM_004949.5):c.60G>A (p.L20=)
ISCN -
DB-ID DSC1_000013
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.*28810G>A r.(=) p.(=) -
DSC2 NM_004949.3 -?/. - c.60G>A r.(?) p.(=) -


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