Variant #0000865367 (NC_000017.10:g.4927205G>A, NM_006612.5:c.3071G>A (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.4927205G>A
DNA change (hg38) -
Published as KIF1C(NM_006612.5):c.3071G>A (p.R1024Q), KIF1C(NM_006612.6):c.3071G>A (p.R1024Q)
ISCN -
DB-ID KIF1C_000020 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) 0.00185 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 2022-05-09 16:01:56 +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.3071G>A r.(?) p.(Arg1024Gln)


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