Variant #0000722535 (NC_000009.11:g.37782012_37782013insGGCTT, NM_016042.3:c.596_597insAAGCC (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.37782012_37782013insGGCTT
DNA change (hg38) -
Published as EXOSC3(NM_016042.3):c.596_597insAAGCC (p.F200Sfs*5)
ISCN -
DB-ID EXOSC3_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EXOSC3 NM_016042.3 ?/. - c.596_597insAAGCC r.(?) p.(Phe200Serfs*5)
TRMT10B NM_144964.2 ?/. - c.*4308_*4309insGGCTT r.(=) p.(=)


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