Variant #0000253585 (NC_000010.10:g.70748666A>G, NM_015634.3:c.78A>G (KIAA1279))

Chromosome 10
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.70748666A>G
DNA change (hg38) g.68988910A>G
Published as KIF1BP(NM_015634.3):c.78A>G (p.K26=)
ISCN -
DB-ID KIAA1279_000003
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) 0.00185 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-27 14:17:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX21 NM_004728.3 -/. - c.*6098A>G r.(=) p.(=)
KIAA1279 NM_015634.3 -/. - c.78A>G r.(?) p.(Lys26=)


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