ClinVar Miner

List of variants in gene DLG3 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_021120.4(DLG3):c.304G>A (p.Gly102Ser) rs11797456 0.00385
NM_021120.4(DLG3):c.429C>T (p.Phe143=) rs144225009 0.00123
NM_021120.4(DLG3):c.2076C>T (p.Ile692=) rs535820581 0.00026
NM_021120.4(DLG3):c.1388C>T (p.Ala463Val) rs371545673 0.00018
NM_021120.4(DLG3):c.2295G>A (p.Lys765=) rs200152610 0.00013
NM_021120.4(DLG3):c.573G>A (p.Val191=) rs200883696 0.00011
NM_021120.4(DLG3):c.873C>T (p.His291=) rs370169893 0.00006
NM_021120.4(DLG3):c.126T>A (p.Gly42=) rs982660834 0.00004
NM_021120.4(DLG3):c.1281C>T (p.Arg427=) rs1473465948 0.00002
NM_021120.4(DLG3):c.2438C>T (p.Ser813Phe) rs140208240 0.00002
NM_021120.4(DLG3):c.1138T>C (p.Phe380Leu) rs749973560 0.00001
NM_021120.4(DLG3):c.94G>A (p.Asp32Asn) rs1373830243 0.00001
NM_021120.4(DLG3):c.1172A>G (p.Lys391Arg) rs1555961844
NM_021120.4(DLG3):c.1242C>T (p.Ile414=) rs797045524
NM_021120.4(DLG3):c.1405+5_1405+7del rs797045525

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.