Variant #0000677176 (NC_000004.11:g.122725850C>G, NM_001034194.1:c.458C>G (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.122725850C>G
DNA change (hg38) -
Published as EXOSC9(NM_001034194.1):c.458C>G (p.A153G)
ISCN -
DB-ID CCNA2_000010
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) 3.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.458C>G r.(?) p.(Ala153Gly)
CCNA2 NM_001237.3 -?/. - c.*12943G>C r.(=) p.(=)


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