Variant #0000976093 (NC_000004.11:g.122734380dup, NC_000004.11(NM_001034194.1):c.828-9dup (EXOSC9))

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.122734380dup
DNA change (hg38) -
Published as EXOSC9(NM_005033.3):c.828-9dup
ISCN -
DB-ID CCNA2_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
EXOSC9 NM_001034194.1 -?/. - c.828-9dup r.(=) p.(=)
CCNA2 NM_001237.3 -?/. - c.*4417dup r.(?) p.(=)


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