Variant #0000979098 (NC_000010.10:g.70776000_70776001del, NM_015634.3:c.1694_1695del (KIAA1279))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.70776000_70776001del
DNA change (hg38) -
Published as KIF1BP(NM_015634.4):c.1694_1695del (p.(Glu565Alafs*16))
ISCN -
DB-ID KIAA1279_000031
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA1279 NM_015634.3 ?/. - c.1694_1695del r.(?) p.(Glu565Alafs*16)


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