Variant #0000861698 (NC_000009.11:g.37780719G>A, NM_016042.3:c.785C>T (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.37780719G>A
DNA change (hg38) -
Published as EXOSC3(NM_016042.3):c.785C>T (p.S262L)
ISCN -
DB-ID EXOSC3_000016
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) 4.0E-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 2022-05-09 15:51:19 +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.785C>T r.(?) p.(Ser262Leu)
TRMT10B NM_144964.2 -?/. - c.*3015G>A r.(=) p.(=)


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