Variant #0001031632 (NC_000001.10:g.21042050G>C, NM_020816.2:c.314C>G (KIF17))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21042050G>C
DNA change (hg38) -
Published as KIF17(NM_001122819.3):c.314C>G (p.(Pro105Arg))
ISCN -
DB-ID KIF17_000005
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) 0.00018 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 2025-05-05 21:14:00 +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     
SH2D5 NM_001103160.1 ?/. - c.*6235C>G r.(=) p.(=)
KIF17 NM_020816.2 ?/. - c.314C>G r.(?) p.(Pro105Arg)


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