Variant #0000983008 (NC_000018.9:g.29126108T>G, NM_001943.3:c.2759T>G (DSG2))

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.29126108T>G
DNA change (hg38) -
Published as DSG2(NM_001943.3):c.2759T>G (p.V920G), DSG2(NM_001943.5):c.2759T>G (p.V920G, p.(Val920Gly)), DSG2-AS1(NR_045216.1):n.1346-239A>C
ISCN -
DB-ID DSG2_000055 See all 8 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) 0.00361 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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     
DSG2 NM_001943.3 -?/. - c.2759T>G r.(?) p.(Val920Gly) -


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