Variant #0000562309 (NC_000017.10:g.5338269T>C, NM_002532.4:c.-15299A>G (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.5338269T>C
DNA change (hg38) g.5434949T>C
Published as C1QBP(NM_001212.3):c.401A>G (p.(Asn134Ser))
ISCN -
DB-ID C1QBP_000001
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) 4.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPAIN NM_001033002.3 ?/. - c.*2378T>C r.(=) p.(=)
C1QBP NM_001212.3 ?/. - c.401A>G r.(?) p.(Asn134Ser)
NUP88 NM_002532.4 ?/. - c.-15299A>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.