Variant #0000791689 (NC_000010.10:g.79581781G>A, DLG5(NM_004747.3):c.2461C>T)

Individual ID 00377591
Chromosome 10
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.79581781G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID DLG5_000009
Variant remarks -
Reference PubMed: Marquez 2021
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLG5 NM_004747.3 +?/. - c.2461C>T r.(?) p.(Arg821*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000378795 DNA SEQ;SEQ-NG - - - 1 Johan den Dunnen