Variant #0000404217 (NC_000005.9:g.36976512_36976514del, NIPBL(NM_133433.3):c.1495+8_1495+10del)

Individual ID 00179804
Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36976512_36976514del
DNA change (hg38) g.36976410_36976412del
Published as 1495+8_1495+10delAAT
ISCN -
DB-ID NIPBL_000219 See all 3 reported entries
Variant remarks not pathogenic, inherited from unaffected father
Reference Redeker (unpublished)
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/PolyPhenScore     
NIPBL NM_133433.3 -/. 9i c.1495+8_1495+10del r.(?) p.(?) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000180707 DNA DHPLC - - NIPBL 1 Bert Redeker