Variant #0000564389 (NC_000018.9:g.28672148C>T, NM_004949.3:c.270G>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.28672148C>T
DNA change (hg38) g.31092185C>T
Published as DSC2(NM_004949.3):c.270G>A (p.E90=), DSC2(NM_004949.5):c.270G>A (p.E90=), DSC2(NM_024422.4):c.270G>A (p.E90=)
ISCN -
DB-ID DSC2_000173 See all 5 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) 0.0005 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 2024-08-28 13:16:32 +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.270G>A r.(?) p.(Glu90=) -


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