Variant #0000337609 (NC_000002.11:g.241689833G>A, NC_000002.11(NM_004321.6):c.2674+13C>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.241689833G>A
DNA change (hg38) g.240750416G>A
Published as KIF1A(NM_001244008.1):c.2977+13C>T, KIF1A(NM_001244008.2):c.2977+13C>T
ISCN -
DB-ID KIF1A_000057 See all 7 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) 0.02099 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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.2977+13C>T r.(=) p.(=)
KIF1A NM_004321.6 -/. - c.2674+13C>T r.(=) p.(=)


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