Variant #0000978783 (NC_000009.11:g.86615956C>T, NM_002140.3:c.-20646G>A (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.86615956C>T
DNA change (hg38) -
Published as RMI1(NM_001358291.2):c.55C>T (p.(His19Tyr))
ISCN -
DB-ID HNRNPK_000022
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) 0.00091 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 2024-04-19 20:27:30 +02:00 (CEST)
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.-20646G>A r.(?) p.(=)
RMI1 NM_024945.2 -?/. - c.55C>T r.(?) p.(His19Tyr)


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