Variant #0000863717 (NC_000014.8:g.92537354_92537355insTGCTGCTGCTG, ATXN3(NM_004993.5):c.915_916insCAGCAGCAGCA)

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.92537354_92537355insTGCTGCTGCTG
DNA change (hg38) -
Published as ATXN3(NM_004993.5):c.915_916insCAGCAGCAGCA (p.G306Qfs*29)
ISCN -
DB-ID ATXN3_000086
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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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_916insCAGCAGCAGCA - r.(?) p.(Gly306Glnfs*29)