ClinVar Miner

List of variants reported for Autistic behavior; Moderate global developmental delay by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
GRCh37/hg19 2q24.2(chr2:161967492-162428730)
NM_006593.4(TBR1):c.1155C>G (p.Asn385Lys) rs762713626
NM_006593.4(TBR1):c.1177dup (p.Asp393fs) rs1553510680
NM_006593.4(TBR1):c.1369_1371delinsCA (p.Thr457fs) rs1553511175
NM_006593.4(TBR1):c.1588_1594dup (p.Thr532fs) rs869312704
NM_006593.4(TBR1):c.471del (p.Ala156_Tyr157insTer) rs1553510171
NM_006593.4(TBR1):c.713_719del (p.Ser238fs) rs1553510280
NM_006593.4(TBR1):c.844C>T (p.Gln282Ter) rs1553510313
NM_006593.4(TBR1):c.896G>A (p.Trp299Ter) rs1553510385
Single allele

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.