Variant #0001029686 (NC_000007.13:g.70228044A>G, NM_015570.2:c.931A>G (AUTS2))

Chromosome 7
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.70228044A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID AUTS2_000176
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1302553938
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-02-25 17:04:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AUTS2 NM_015570.2 -?/. - c.931A>G r.(?) p.(Thr311Ala)


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