Variant #0000612129 (NC_000009.11:g.37783957_37783960del, NM_016042.3:c.428_431del (EXOSC3))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37783957_37783960del
DNA change (hg38) g.37783960_37783963del
Published as EXOSC3(NM_001002269.2):c.428_431del (p.(Tyr143CysfsTer82))
ISCN -
DB-ID EXOSC3_000011
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-25 14:01:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC3 NM_016042.3 +?/. - c.428_431del r.(?) p.(Tyr143CysfsTer59)
TRMT10B NM_144964.2 +?/. - c.*6253_*6256del r.(=) p.(=)


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