Variant #0000969361 (NC_000018.9:g.29078229G>C, NM_001943.3:c.15G>C (DSG2))

Chromosome 18
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.29078229G>C
DNA change (hg38) -
Published as DSG2(NM_001943.3):c.15G>C (p.P5=), DSG2(NM_001943.5):c.15G>C (p.P5=)
ISCN -
DB-ID DSG2_000395 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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.15G>C r.(?) p.(Pro5=) -


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