ClinVar Miner

List of variants in gene DLL4 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 102
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_019074.4(DLL4):c.67-20C>T rs3212277 0.02146
NM_019074.4(DLL4):c.2053-170G>A rs56038127 0.02073
NM_019074.4(DLL4):c.*304C>T rs56400389 0.01649
NM_019074.4(DLL4):c.1239C>T (p.Asn413=) rs35748882 0.01422
NM_019074.4(DLL4):c.1944-86C>A rs78015452 0.00735
NM_019074.4(DLL4):c.369C>T (p.His123=) rs187700175 0.00244
NM_019074.4(DLL4):c.1005T>C (p.Asn335=) rs202220884 0.00054
NM_019074.4(DLL4):c.743G>A (p.Arg248Gln) rs139491690 0.00051
NM_019074.4(DLL4):c.938G>A (p.Arg313His) rs146665183 0.00047
NM_019074.4(DLL4):c.1386C>T (p.Leu462=) rs374717233 0.00039
NM_019074.4(DLL4):c.68G>A (p.Arg23His) rs370744960 0.00036
NM_019074.4(DLL4):c.897G>A (p.Thr299=) rs374507826 0.00033
NM_019074.4(DLL4):c.398C>A (p.Ala133Asp) rs370487005 0.00020
NM_019074.4(DLL4):c.156C>T (p.Pro52=) rs367900130 0.00011
NM_019074.4(DLL4):c.969G>A (p.Leu323=) rs374508526 0.00011
NM_019074.4(DLL4):c.1329C>T (p.Asp443=) rs751697404 0.00009
NM_019074.4(DLL4):c.1971G>A (p.Ala657=) rs369676256 0.00009
NM_019074.4(DLL4):c.1353C>T (p.His451=) rs368013738 0.00007
NM_019074.4(DLL4):c.1326C>T (p.Ser442=) rs750346321 0.00006
NM_019074.4(DLL4):c.1943+18G>T rs748004538 0.00005
NM_019074.4(DLL4):c.1158T>C (p.Tyr386=) rs762170748 0.00004
NM_019074.4(DLL4):c.469T>C (p.Leu157=) rs776768540 0.00004
NM_019074.4(DLL4):c.2052+18C>T rs1438467184 0.00002
NM_019074.4(DLL4):c.395-19C>T rs755628140 0.00002
NM_019074.4(DLL4):c.534C>T (p.Asn178=) rs753354782 0.00002
NM_019074.4(DLL4):c.67-10T>C rs1249140063 0.00002
NM_019074.4(DLL4):c.1209G>A (p.Val403=) rs757134925 0.00001
NM_019074.4(DLL4):c.1347C>T (p.Cys449=) rs752793079 0.00001
NM_019074.4(DLL4):c.1728G>A (p.Lys576=) rs776732603 0.00001
NM_019074.4(DLL4):c.2034A>G (p.Glu678=) rs748516151 0.00001
NM_019074.4(DLL4):c.337-10C>T rs372529945 0.00001
NM_019074.4(DLL4):c.499C>T (p.Leu167=) rs1468519974 0.00001
NM_019074.4(DLL4):c.-105C>G rs111494897
NM_019074.4(DLL4):c.1020+14C>G
NM_019074.4(DLL4):c.1020+14C>T rs372257089
NM_019074.4(DLL4):c.1020+15A>C
NM_019074.4(DLL4):c.1077T>C (p.Cys359=)
NM_019074.4(DLL4):c.1122G>C (p.Gly374=)
NM_019074.4(DLL4):c.1134G>C (p.Arg378=)
NM_019074.4(DLL4):c.1197C>T (p.Cys399=)
NM_019074.4(DLL4):c.1241-8C>A
NM_019074.4(DLL4):c.1281C>T (p.Arg427=)
NM_019074.4(DLL4):c.12G>A (p.Ala4=)
NM_019074.4(DLL4):c.1317C>T (p.Leu439=)
NM_019074.4(DLL4):c.1320C>T (p.His440=)
NM_019074.4(DLL4):c.1404C>T (p.Ala468=)
NM_019074.4(DLL4):c.1413T>C (p.Ser471=) rs942527179
NM_019074.4(DLL4):c.1416C>G (p.Gly472=)
NM_019074.4(DLL4):c.1418G>A (p.Arg473Gln)
NM_019074.4(DLL4):c.1431G>T (p.Val477=)
NM_019074.4(DLL4):c.1458G>A (p.Ser486=)
NM_019074.4(DLL4):c.1506C>T (p.Asp502=)
NM_019074.4(DLL4):c.1552G>A (p.Glu518Lys)
NM_019074.4(DLL4):c.1560C>T (p.Pro520=)
NM_019074.4(DLL4):c.1599G>A (p.Ser533=)
NM_019074.4(DLL4):c.1635G>A (p.Leu545=)
NM_019074.4(DLL4):c.1668G>T (p.Arg556=)
NM_019074.4(DLL4):c.1683C>T (p.Asp561=)
NM_019074.4(DLL4):c.1707C>T (p.Asn569=)
NM_019074.4(DLL4):c.1716G>A (p.Ser572=)
NM_019074.4(DLL4):c.1734C>T (p.Asn578=)
NM_019074.4(DLL4):c.1806G>A (p.Lys602=)
NM_019074.4(DLL4):c.1836A>T (p.Thr612=)
NM_019074.4(DLL4):c.18G>A (p.Arg6=)
NM_019074.4(DLL4):c.1932G>A (p.Leu644=)
NM_019074.4(DLL4):c.1933C>A (p.Arg645=)
NM_019074.4(DLL4):c.1944-12G>A
NM_019074.4(DLL4):c.1944-17G>A
NM_019074.4(DLL4):c.1950G>A (p.Lys650=)
NM_019074.4(DLL4):c.1984A>C (p.Arg662=)
NM_019074.4(DLL4):c.2049G>A (p.Thr683=)
NM_019074.4(DLL4):c.204C>A (p.Val68=)
NM_019074.4(DLL4):c.2052+15C>T
NM_019074.4(DLL4):c.2053-13C>T
NM_019074.4(DLL4):c.205G>T (p.Val69Phe)
NM_019074.4(DLL4):c.297G>C (p.Gly99=)
NM_019074.4(DLL4):c.315G>A (p.Leu105=)
NM_019074.4(DLL4):c.336+11C>T
NM_019074.4(DLL4):c.336+8C>A
NM_019074.4(DLL4):c.337-6del rs1892754326
NM_019074.4(DLL4):c.375A>G (p.Pro125=)
NM_019074.4(DLL4):c.395-6C>T rs753772817
NM_019074.4(DLL4):c.441C>G (p.Gly147=)
NM_019074.4(DLL4):c.522C>T (p.Ile174=) rs2140369225
NM_019074.4(DLL4):c.576T>C (p.Asn192=)
NM_019074.4(DLL4):c.582C>T (p.His194=) rs1596192583
NM_019074.4(DLL4):c.585C>T (p.Phe195=)
NM_019074.4(DLL4):c.595G>C (p.Val199Leu)
NM_019074.4(DLL4):c.658+10C>G rs1373670380
NM_019074.4(DLL4):c.659-20G>C
NM_019074.4(DLL4):c.66+55C>T rs115657051
NM_019074.4(DLL4):c.708A>C (p.Pro236=) rs753025345
NM_019074.4(DLL4):c.719+14A>G
NM_019074.4(DLL4):c.720-16C>G
NM_019074.4(DLL4):c.720-4C>G
NM_019074.4(DLL4):c.720-9G>C
NM_019074.4(DLL4):c.753C>T (p.Asn251=)
NM_019074.4(DLL4):c.850+10G>C
NM_019074.4(DLL4):c.851-10G>A
NM_019074.4(DLL4):c.851-10G>T
NM_019074.4(DLL4):c.851-209del rs561583510
NM_019074.4(DLL4):c.891G>T (p.Gly297=) rs1246826200

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.