Variant #0001055790 (NC_000017.10:g.5308552A>G, NM_002532.4:c.869T>C (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.5308552A>G
DNA change (hg38) -
Published as NUP88(NM_002532.6):c.869T>C (p.(Ile290Thr))
ISCN -
DB-ID NUP88_000010
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPAIN NM_001033002.3 ?/. - c.-14979A>G r.(?) p.(=)
NUP88 NM_002532.4 ?/. - c.869T>C r.(?) p.(Ile290Thr)
RABEP1 NM_004703.4 ?/. - c.*22034A>G r.(=) p.(=)


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