Variant #0000716647 (NC_000001.10:g.10363487T>C, NC_000001.10(NM_015074.3):c.1977+6183T>C (KIF1B))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10363487T>C
DNA change (hg38) -
Published as KIF1B(NM_001365953.1):c.2244T>C (p.A748=), KIF1B(NM_183416.4):c.2244T>C (p.A748=)
ISCN -
DB-ID KIF1B_000028 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) 0.00348 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF1B NM_015074.3 -?/. - c.1977+6183T>C r.(=) p.(=)


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