Variant #0000564363 (NC_000018.9:g.28666616G>A, NM_004949.3:c.865C>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.28666616G>A
DNA change (hg38) g.31086653G>A
Published as DSC2(NM_004949.3):c.865C>T (p.P289S), DSC2(NM_004949.5):c.865C>T (p.P289S), DSC2(NM_024422.4):c.865C>T (p.P289S)
ISCN -
DB-ID DSC2_000009 See all 6 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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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.865C>T r.(?) p.(Pro289Ser) -


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