Variant #0001041989 (NC_000017.10:g.5257669_5257671del, NM_002532.4:c.*31860_*31862del (NUP88))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.5257669_5257671del
DNA change (hg38) -
Published as RABEP1(NM_004703.6):c.979_981del (p.(Gln327del))
ISCN -
DB-ID NUP88_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
NUP88 NM_002532.4 ?/. - c.*31860_*31862del r.(=) p.(=)
RABEP1 NM_004703.4 ?/. - c.979_981del r.(?) p.(Gln327del)


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