Variant #0000894043 (NC_000017.10:g.4904113C>T, NM_006612.5:c.153C>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.4904113C>T
DNA change (hg38) -
Published as KIF1C(NM_006612.6):c.153C>T (p.T51=)
ISCN -
DB-ID INCA1_000009
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) 0.00061 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 2022-11-01 13:41:49 +01:00 (CET)
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.153C>T r.(?) p.(Thr51=)
INCA1 NM_213726.2 -?/. - c.-3650G>A r.(?) p.(=)


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