Variant #0000852322 (NC_000009.11:g.86586235T>C, NM_002140.3:c.1045A>G (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.86586235T>C
DNA change (hg38) -
Published as HNRNPK(NM_002140.5):c.1045A>G (p.I349V)
ISCN -
DB-ID HNRNPK_000016
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.1045A>G r.(?) p.(Ile349Val)
RMI1 NM_024945.2 ?/. - c.-9810T>C r.(?) p.(=)


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