Variant #0000889325 (NC_000010.10:g.94368954C>T, NM_004523.3:c.565C>T (KIF11))

Chromosome 10
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.94368954C>T
DNA change (hg38) -
Published as KIF11(NM_004523.3):c.565C>T (p.(Arg189Cys)), KIF11(NM_004523.4):c.565C>T (p.R189C)
ISCN -
DB-ID KIF11_000106 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +01:00 (CET)
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     
KIF11 NM_004523.3 ?/. - c.565C>T r.(?) p.(Arg189Cys)


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