Variant #0000553415 (NC_000014.8:g.92537379_92537380insGCTGCTGCTGCTGCTGCTGCTGC, ATXN3(NM_004993.5):c.890_891insGCAGCAGCAGCAGCAGCAGCAGC)

Chromosome 14
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.92537379_92537380insGCTGCTGCTGCTGCTGCTGCTGC
DNA change (hg38) g.92071035_92071036insGCTGCTGCTGCTGCTGCTGCTGC
Published as ATXN3(NM_004993.5):c.890_891insGCAGCAGCAGCAGCAGCAGCAGC (p.Q305Hfs*34), ATXN3(NM_004993.6):c.890_891insGCAGCAGCAGCAGCAGCAGCAGC (p.Q305Hfs*34)
ISCN -
DB-ID ATXN3_000059 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATXN3 NM_004993.5 -?/. - c.890_891insGCAGCAGCAGCAGCAGCAGCAGC - r.(?) p.(Gln305HisfsTer34)