Variant #0000515333 (NC_000002.11:g.241679464A>G, NC_000002.11(NM_004321.6):c.3598+11T>C (KIF1A))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.241679464A>G
DNA change (hg38) g.240740047A>G
Published as KIF1A(NM_001244008.2):c.3901+11T>C
ISCN -
DB-ID KIF1A_000040 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) 0.01294 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
KIF1A NM_001244008.1 -/. - c.3901+11T>C r.(=) p.(=)
KIF1A NM_004321.6 -/. - c.3598+11T>C r.(=) p.(=)


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