Variant #0001053253 (NC_000009.11:g.37782118T>C, NM_016042.3:c.491A>G (EXOSC3))

Chromosome 9
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.37782118T>C
DNA change (hg38) -
Published as EXOSC3(NM_016042.4):c.491A>G (p.(Tyr164Cys))
ISCN -
DB-ID EXOSC3_000024
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) 1.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
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.491A>G r.(?) p.(Tyr164Cys)
TRMT10B NM_144964.2 ?/. - c.*4414T>C r.(=) p.(=)


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