Variant #0000621332 (NC_000004.11:g.104117435_104117437del, NC_000004.11(NM_001813.2):c.149-6_149-4del (CENPE))

Chromosome 4
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.104117435_104117437del
DNA change (hg38) g.103196278_103196280del
Published as CENPE(NM_001813.3):c.149-6_149-4delGTT
ISCN -
DB-ID CENPE_000008 See all 2 reported entries
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-16 14:08:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPE NM_001813.2 -?/. - c.149-6_149-4del r.spl? p.?


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