Variant #0001037541 (NC_000009.11:g.37783990T>G, NM_016042.3:c.395A>C (EXOSC3))

Chromosome 9
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.37783990T>G
DNA change (hg38) -
Published as EXOSC3(NM_016042.3):c.395A>C (p.D132A), EXOSC3(NM_016042.4):c.395A>C (p.(Asp132Ala), p.D132A)
ISCN -
DB-ID EXOSC3_000001 See all 21 reported entries
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) 0.00038 View details
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     
EXOSC3 NM_016042.3 +/. - c.395A>C r.(?) p.(Asp132Ala)


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