Variant #0001034301 (NC_000004.11:g.122739218_122739222del, NM_001034194.1:c.*1207_*1211del (EXOSC9))

Chromosome 4
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.122739218_122739222del
DNA change (hg38) -
Published as CCNA2(NM_001237.5):c.1229_1233del (p.(Arg410Lysfs*46))
ISCN -
DB-ID CCNA2_000019
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 2025-05-05 21:14:00 +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.*1207_*1211del r.(=) p.(=)
CCNA2 NM_001237.3 ?/. - c.1229_1233del r.(?) p.(Arg410Lysfs*46)


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