Variant #0000604623 (NC_000001.10:g.10381887A>G, NM_015074.3:c.2192A>G (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.10381887A>G
DNA change (hg38) g.10321829A>G
Published as KIF1B(NM_001365951.3):c.2330A>G (p.N777S), KIF1B(NM_015074.3):c.2192A>G (p.(Asn731Ser))
ISCN -
DB-ID KIF1B_000085 See all 4 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) 0.00474 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +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.2192A>G r.(?) p.(Asn731Ser)


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