Variant #0000808105 (NC_000017.10:g.4925475C>T, NM_006612.5:c.2099C>T (KIF1C))

Chromosome 17
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.4925475C>T
DNA change (hg38) -
Published as KIF1C(NM_006612.5):c.2099C>T (p.P700L), KIF1C(NM_006612.6):c.2099C>T (p.P700L)
ISCN -
DB-ID KIF1C_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) 0.00285 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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     
KIF1C NM_006612.5 -?/. - c.2099C>T r.(?) p.(Pro700Leu)


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