Variant #0000525828 (NC_000005.9:g.54527468dup, NM_021147.3:c.793dup (CCNO))

Chromosome 5
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.54527468dup
DNA change (hg38) g.55231640dup
Published as CCNO(NM_021147.5):c.793dupG (p.V265Gfs*106)
ISCN -
DB-ID CCNO_000014
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MCIN NM_001190787.1 +/. - c.-4497dup r.(?) p.(=)
CCNO NM_021147.3 +/. - c.793dup r.(?) p.(Val265GlyfsTer106)


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