Variant #0000261327 (NC_000003.11:g.63968134T>A, NC_000003.11(NM_000333.3):c.1012+13T>A (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.63968134T>A
DNA change (hg38) g.63982458T>A
Published as ATXN7(NM_000333.3):c.1012+13T>A, ATXN7(NM_000333.4):c.1012+13T>A
ISCN -
DB-ID ATXN7_000033 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) 0.00054 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
ATXN7 NM_000333.3 -?/. - c.1012+13T>A - r.(=) p.(=)


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