Variant #0000930421 (NC_000015.9:g.69732419_69732422del, NC_000015.9(NM_004856.5):c.1887+3_1887+6del (KIF23))

Chromosome 15
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.69732419_69732422del
DNA change (hg38) -
Published as KIF23(NM_138555.4):c.1887+3_1887+6delGAGT
ISCN -
DB-ID KIF23_000013
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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     
KIF23 NM_004856.5 ?/. - c.1887+3_1887+6del r.spl? p.?


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