Variant #0000520041 (NC_000003.11:g.47385371C>T, NM_022342.4:c.-61392G>A (KIF9))

Chromosome 3
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.47385371C>T
DNA change (hg38) g.47343881C>T
Published as KLHL18(NM_025010.5):c.1665C>T (p.A555=)
ISCN -
DB-ID KIF9_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-15 08:55:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIF9 NM_022342.4 -?/. - c.-61392G>A r.(?) p.(=)
KLHL18 NM_025010.4 -?/. - c.1665C>T r.(?) p.(Ala555=)


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