Variant #0000329627 (NC_000003.11:g.134214170del, NM_025180.3:c.8del (CEP63))

Chromosome 3
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.134214170del
DNA change (hg38) g.134495328del
Published as CEP63(NM_001353108.3):c.8del (p.(Ala3ValfsTer3))
ISCN -
DB-ID CEP63_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANAPC13 NM_015391.3 ?/. - c.-9404del r.(?) p.(=)
CEP63 NM_025180.3 ?/. - c.8del r.(?) p.(Ala3ValfsTer3)


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