Variant #0000865644 (NC_000018.9:g.29099821G>A, NM_001943.3:c.137G>A (DSG2))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.29099821G>A
DNA change (hg38) -
Published as DSG2(NM_001943.3):c.137G>A (p.R46Q), DSG2(NM_001943.5):c.137G>A (p.R46Q)
ISCN -
DB-ID DSG2_000006 See all 11 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
DSG2 NM_001943.3 +/. - c.137G>A r.(?) p.(Arg46Gln) -


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