Variant #0000164534 (NC_000005.9:g.176637127del, NSD1(NM_022455.4):c.1727del)

Individual ID 00101323
Chromosome 5
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.176637127del
DNA change (hg38) g.177210126del
Published as -
ISCN -
DB-ID NSD1_000009
Variant remarks -
Reference PubMed: Douglas 2003
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     
NSD1 NM_022455.4 +/. 5 c.1727del r.(?) p.(Asn576ThrfsTer23)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000101771 DNA CSGE - - NSD1 1 Johan den Dunnen