Variant #0001033188 (NC_000002.11:g.241752380A>G, NM_004321.6:c.-15211T>C (KIF1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.241752380A>G
DNA change (hg38) -
Published as KIF1A(NM_001244008.2):c.-61+7159T>C
ISCN -
DB-ID KIF1A_000349
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF1A NM_001244008.1 -?/. - c.-61+7159T>C r.(=) p.(=)
KIF1A NM_004321.6 -?/. - c.-15211T>C r.(?) p.(=)


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