Variant #0000548790 (NC_000012.11:g.57963454C>T, NM_004984.2:c.1105C>T (KIF5A))

Chromosome 12
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.57963454C>T
DNA change (hg38) g.57569671C>T
Published as KIF5A(NM_004984.3):c.1105C>T (p.R369W), KIF5A(NM_004984.4):c.1105C>T (p.R369W)
ISCN -
DB-ID KIF5A_000012 See all 5 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) 0.00063 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF5A NM_004984.2 ?/. - c.1105C>T r.(?) p.(Arg369Trp)


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