Variant #0000553392 (NC_000014.8:g.92537353_92537354insG, ATXN3(NM_004993.5):c.916_917insC)

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.92537353_92537354insG
DNA change (hg38) g.92071009_92071010insG
Published as ATXN3(NM_004993.5):c.916_917insC (p.G306Afs*12), ATXN3(NM_004993.6):c.916_917insC (p.G306Afs*12)
ISCN -
DB-ID ATXN3_000043 See all 3 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATXN3 NM_004993.5 -/. - c.916_917insC - r.(?) p.(Gly306AlafsTer12)