Variant #0001035196 (NC_000005.9:g.36952149_36952156dup, NC_000005.9(NM_133433.3):c.-79-1571_-79-1564dup (NIPBL))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36952149_36952156dup
DNA change (hg38) -
Published as NIPBL(NM_133433.4):c.-79-1575_-79-1568dupTGTGTGTG
ISCN -
DB-ID NIPBL_000486
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIPBL NM_133433.3 -?/. - c.-79-1571_-79-1564dup r.(=) p.(=)


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