Variant #0000978784 (NC_000009.11:g.86616711del, NM_002140.3:c.-21400del (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.86616711del
DNA change (hg38) -
Published as RMI1(NM_001358291.2):c.810del (p.(Thr271GlnfsTer36))
ISCN -
DB-ID HNRNPK_000023
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPK NM_002140.3 ?/. - c.-21400del r.(?) p.(=)
RMI1 NM_024945.2 ?/. - c.810del r.(?) p.(Thr271Glnfs*36)


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