Variant #0000275552 (NC_000018.9:g.28681889G>T, NM_004949.3:c.46C>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.28681889G>T
DNA change (hg38) g.31101926G>T
Published as DSC2(NM_024422.4):c.46C>A (p.R16=)
ISCN -
DB-ID DSC2_000177 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 17:40:48 +02:00 (CEST)
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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.*28796C>A r.(=) p.(=) -
DSC2 NM_004949.3 -?/. - c.46C>A r.(?) p.(Arg16=) -


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