Variant #0000267581 (NC_000018.9:g.28991180T>C, DSG4(NM_177986.3):c.2138-14T>C)

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.28991180T>C
DNA change (hg38) g.31411217T>C
Published as DSG4(NM_001134453.3):c.2181T>C (p.H727=)
ISCN -
DB-ID DSG4_000006
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSG4 NM_177986.3 -?/. - c.2138-14T>C r.(=) p.(=)