Variant #0000289147 (NC_000009.11:g.86590381C>T, NM_002140.3:c.253G>A (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.86590381C>T
DNA change (hg38) g.83975466C>T
Published as HNRNPK(NM_002140.4):c.253G>A (p.E85K)
ISCN -
DB-ID HNRNPK_000002 See all 2 reported entries
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPK NM_002140.3 ?/. - c.253G>A r.(?) p.(Glu85Lys)
RMI1 NM_024945.2 ?/. - c.-5664C>T r.(?) p.(=)


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