Variant #0001053274 (NC_000009.11:g.86593370A>G, NC_000009.11(NM_002140.3):c.-107-3T>C (HNRNPK))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.86593370A>G
DNA change (hg38) -
Published as HNRNPK(NM_031263.4):c.-107-3T>C
ISCN -
DB-ID HNRNPK_000026
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 2025-11-01 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     
HNRNPK NM_002140.3 -?/. - c.-107-3T>C r.spl? p.?
RMI1 NM_024945.2 -?/. - c.-2675A>G r.(?) p.(=)


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