Variant #0000694254 (NC_000005.9:g.176637245_176637246del, NSD1(NM_022455.4):c.1845_1846del)

Individual ID 00311480
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.176637245_176637246del
DNA change (hg38) g.177210244_177210245del
Published as 1840_1841delGT
ISCN -
DB-ID NSD1_000390
Variant remarks -
Reference PubMed: Faundes 2018
ClinVar ID -
dbSNP ID -
Origin De novo
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 +/. - c.1845_1846del r.(?) p.(Cys615Trpfs*13)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000312650 DNA SEQ;SEQ-NG - WES NSD1 1 Johan den Dunnen