Variant #0000272854 (NC_000004.11:g.122739985T>C, NM_001034194.1:c.*1974T>C (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.122739985T>C
DNA change (hg38) g.121818830T>C
Published as CCNA2(NM_001237.4):c.1086A>G (p.L362=)
ISCN -
DB-ID CCNA2_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) 0.00029 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 14:42:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC9 NM_001034194.1 -?/. - c.*1974T>C r.(=) p.(=)
CCNA2 NM_001237.3 -?/. - c.1086A>G r.(?) p.(Leu362=)


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