Variant #0000502229 (NC_000001.10:g.10327624dup, NC_000001.10(NM_015074.3):c.608+8dup (KIF1B))

Chromosome 1
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.10327624dup
DNA change (hg38) g.10267566dup
Published as KIF1B(NM_015074.3):c.608+7_608+8insA (p.(=)), KIF1B(NM_015074.3):c.608+8dupA
ISCN -
DB-ID KIF1B_000014 See all 3 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF1B NM_015074.3 -/. - c.608+8dup r.(=) p.(=)


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