Variant #0000515383 (NC_000002.11:g.241725893T>A, NM_004321.6:c.467A>T (KIF1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.241725893T>A
DNA change (hg38) g.240786476T>A
Published as KIF1A(NM_001244008.1):c.467A>T (p.(Asp156Val))
ISCN -
DB-ID KIF1A_000220
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF1A NM_001244008.1 +?/. - c.467A>T r.(?) p.(Asp156Val)
KIF1A NM_004321.6 +?/. - c.467A>T r.(?) p.(Asp156Val)


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