Variant #0000816547 (NC_000007.13:g.69064692C>A, NM_015570.2:c.53C>A (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.69064692C>A
DNA change (hg38) g.69599706C>A
Published as -
ISCN -
DB-ID AUTS2_000117
Variant remarks Heterozygous variant was observed in the product of conception after a spontaneous abortion at gestational week 8 and 3/7
Reference PubMed: Zhao et al., 2021
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
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 15:02:40 +02:00 (CEST)
Date last edited 2021-10-27 09:17:39 +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.53C>A r.(?) p.(Ser18*)


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