Variant #0000852533 (NC_000010.10:g.70765671G>A, NM_015634.3:c.789G>A (KIAA1279))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70765671G>A
DNA change (hg38) -
Published as KIF1BP(NM_015634.4):c.789G>A (p.K263=), KIFBP(NM_015634.4):c.789G>A (p.K263=)
ISCN -
DB-ID KIAA1279_000029
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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:40:45 +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     
KIAA1279 NM_015634.3 +/. - c.789G>A r.(?) p.(Lys263=)


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