Variant #0000816570 (NC_000007.13:g.70228059C>T, NM_015570.2:c.946C>T (AUTS2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70228059C>T
DNA change (hg38) g.70763073C>T
Published as -
ISCN -
DB-ID AUTS2_000119 See all 3 reported entries
Variant remarks childhood-onset dystonia, interpreted as an expansion of the neurodevelopmental clinical spectrum previously associated with this gene
Reference PubMed: Zech et al., 2020
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Alexander Groffen
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Alexander Groffen
Date created 2021-10-26 17:12:46 +02:00 (CEST)
Date last edited 2021-10-27 10:03:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AUTS2 NM_015570.2 +?/+? - c.946C>T r.(?) p.(Arg316*)


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