Variant #0000966883 (NC_000012.11:g.39726207G>A, NM_001173464.1:c.2860C>T (KIF21A))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39726207G>A
DNA change (hg38) -
Published as KIF21A(NM_001173464.2):c.2860C>T (p.(Arg954Trp)), KIF21A(NM_017641.4):c.2821C>T (p.R941W)
ISCN -
DB-ID KIF21A_000016 See all 3 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF21A NM_001173464.1 +/. - c.2860C>T r.(?) p.(Arg954Trp)


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