Variant #0000553399 (NC_000014.8:g.92537354_92537355insTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG, ATXN3(NM_004993.5):c.915_916insCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA)

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.92537354_92537355insTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG
DNA change (hg38) g.92071010_92071011insTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG
Published as ATXN3(NM_004993.5):c.915_916insCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA (p.G306Qfs*36)
ISCN -
DB-ID ATXN3_000047
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 2020-07-05 16:40:20 +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.915_916insCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA - r.(?) p.(Gly306GlnfsTer36)