Variant #0000888862 (NC_000009.11:g.37783955A>G, NM_016042.3:c.430T>C (EXOSC3))

Chromosome 9
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.37783955A>G
DNA change (hg38) -
Published as EXOSC3(NM_016042.3):c.430T>C (p.L144=), EXOSC3(NM_016042.4):c.430T>C (p.L144=)
ISCN -
DB-ID EXOSC3_000013 See all 2 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) 0.00027 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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.430T>C r.(?) p.(Leu144=)
TRMT10B NM_144964.2 -?/. - c.*6251A>G r.(=) p.(=)


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