Variant #0001046213 (NC_000009.11:g.86588263G>A, NM_002140.3:c.454C>T (HNRNPK))

Chromosome 9
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.86588263G>A
DNA change (hg38) -
Published as HNRNPK(NM_002140.4):c.454C>T (p.H152Y)
ISCN -
DB-ID HNRNPK_000025
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 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPK NM_002140.3 ?/. - c.454C>T r.(?) p.(His152Tyr)
RMI1 NM_024945.2 ?/. - c.-7782G>A r.(?) p.(=)


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