Variant #0001064723 (NC_000007.13:g.70198963_70198964insA, NC_000007.13(NM_015570.2):c.743-28893_743-28892insA (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.70198963_70198964insA
DNA change (hg38) -
Published as AUTS2(NM_015570.4):c.743-28893_743-28892insA
ISCN -
DB-ID chr7_007636
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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.743-28893_743-28892insA r.(=) p.(=)


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