Variant #0000520572 (NC_000003.11:g.63898392_63898393insAGCAGCCGC, NM_000333.3:c.118_119insAGCAGCCGC (ATXN7))

Chromosome 3
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.63898392_63898393insAGCAGCCGC
DNA change (hg38) g.63912716_63912717insAGCAGCCGC
Published as ATXN7(NM_000333.4):c.118_119insAGCAGCCGC (p.Q39_P40insQQP), ATXN7(NM_001377405.1):c.118_119insAGCAGCCGC (p.(Gln39_Pro40insGlnGlnPro))
ISCN -
DB-ID ATXN7_000047 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
ATXN7 NM_000333.3 -?/. - c.118_119insAGCAGCCGC - r.(?) p.(Gln39_Pro40insGlnGlnPro)


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