Variant #0000914898 (NC_000017.10:g.5336594C>A, NM_002532.4:c.-13624G>T (NUP88))

Chromosome 17
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.5336594C>A
DNA change (hg38) -
Published as C1QBP(NM_001212.4):c.699+19G>T
ISCN -
DB-ID C1QBP_000005
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) 0.00581 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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.*703C>A r.(=) p.(=)
C1QBP NM_001212.3 -/. - c.699+19G>T r.(=) p.(=)
NUP88 NM_002532.4 -/. - c.-13624G>T r.(?) p.(=)


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