Variant #0000278546 (NC_000002.11:g.241686737G>A, NM_001244008.1:c.2979C>T (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.241686737G>A
DNA change (hg38) g.240747320G>A
Published as KIF1A(NM_001244008.1):c.2979C>T (p.A993=), KIF1A(NM_001244008.2):c.2979C>T (p.A993=)
ISCN -
DB-ID KIF1A_000020 See all 4 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) 0.00391 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 2018-01-15 20:58:59 +01:00 (CET)
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.2979C>T r.(?) p.(Ala993=)
KIF1A NM_004321.6 -/. - c.2676C>T r.(?) p.(Ala892=)


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