Variant #0000806055 (NC_000013.10:g.25486147_25486148del, NM_018451.3:c.505_506del (CENPJ))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25486147_25486148del
DNA change (hg38) -
Published as CENPJ(NM_018451.4):c.505_506delCA (p.Q169Efs*27)
ISCN -
DB-ID CENPJ_000109
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 2021-09-17 14:40:49 +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     
CENPJ NM_018451.3 +/. - c.505_506del r.(?) p.(Gln169Glufs*27)


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