Variant #0000997978 (NC_000009.11:g.86592624G>A, NM_002140.3:c.136C>T (HNRNPK))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.86592624G>A
DNA change (hg38) -
Published as HNRNPK(NM_002140.4):c.136C>T (p.R46C), HNRNPK(NM_002140.5):c.136C>T (p.R46C)
ISCN -
DB-ID HNRNPK_000007 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +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.136C>T r.(?) p.(Arg46Cys)
RMI1 NM_024945.2 +?/. - c.-3421G>A r.(?) p.(=)


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