Variant #0000404192 (NC_000005.9:g.36976284_36976287del, NIPBL(NM_133433.3):c.1275_1278del)

Individual ID 00179779
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.36976284_36976287del
DNA change (hg38) g.36976182_36976185del
Published as 1275_1278delAACA
ISCN -
DB-ID NIPBL_000196
Variant remarks -
Reference Redeker; PubMed: Oliveira 2010
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 Bert Redeker
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Jorge Oliveira
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/PolyPhenScore     
NIPBL NM_133433.3 +/. 9 c.1275_1278del r.(?) p.(Thr426Hisfs*54) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000180682 DNA DHPLC - - NIPBL 1 Bert Redeker