ClinVar Miner

List of variants in gene DLL4 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_019074.4(DLL4):c.1270C>A (p.Arg424Ser) rs373338394 0.00016
NM_019074.4(DLL4):c.472G>A (p.Asp158Asn) rs145914797 0.00014
NM_019074.4(DLL4):c.1873G>A (p.Gly625Arg) rs374530606 0.00012
NM_019074.4(DLL4):c.671C>T (p.Ser224Leu) rs368322432 0.00011
NM_019074.4(DLL4):c.1658G>A (p.Arg553Gln) rs375688749 0.00007
NM_019074.4(DLL4):c.1321G>A (p.Val441Ile) rs374162819 0.00004
NM_019074.4(DLL4):c.1933C>T (p.Arg645Trp) rs376834211 0.00004
NM_019074.4(DLL4):c.1280G>A (p.Arg427His) rs771130564 0.00003
NM_019074.4(DLL4):c.1421G>A (p.Arg474His) rs1407250599 0.00003
NM_019074.4(DLL4):c.937C>T (p.Arg313Cys) rs959903939 0.00003
NM_019074.4(DLL4):c.1132C>T (p.Arg378Trp) rs777108179 0.00002
NM_019074.4(DLL4):c.1895C>T (p.Pro632Leu) rs775051666 0.00002
NM_019074.4(DLL4):c.55C>T (p.Leu19Phe) rs370892158 0.00002
NM_019074.4(DLL4):c.926C>T (p.Thr309Ile) rs199881505 0.00002
NM_019074.4(DLL4):c.1064A>G (p.Tyr355Cys) rs866827922 0.00001
NM_019074.4(DLL4):c.1337G>A (p.Arg446His) rs781379364 0.00001
NM_019074.4(DLL4):c.1670T>G (p.Leu557Arg) rs776875287 0.00001
NM_019074.4(DLL4):c.1870C>T (p.Arg624Trp) rs754788022 0.00001
NM_019074.4(DLL4):c.381C>A (p.Asp127Glu) rs780722090 0.00001
NM_019074.4(DLL4):c.557G>A (p.Arg186His) rs201505624 0.00001
NM_019074.4(DLL4):c.59G>T (p.Trp20Leu) rs1415482653 0.00001
NM_019074.4(DLL4):c.742C>T (p.Arg248Trp) rs540364384 0.00001
NM_019074.4(DLL4):c.1001G>A (p.Arg334His) rs781059377
NM_019074.4(DLL4):c.1025A>G (p.Gln342Arg)
NM_019074.4(DLL4):c.1088C>T (p.Thr363Ile)
NM_019074.4(DLL4):c.1109C>G (p.Pro370Arg) rs777481123
NM_019074.4(DLL4):c.1138C>T (p.Arg380Cys)
NM_019074.4(DLL4):c.1143C>G (p.Asn381Lys) rs1359929548
NM_019074.4(DLL4):c.1154A>C (p.Asn385Thr)
NM_019074.4(DLL4):c.1186G>A (p.Gly396Ser)
NM_019074.4(DLL4):c.1198G>A (p.Glu400Lys)
NM_019074.4(DLL4):c.1229C>T (p.Pro410Leu) rs2140370935
NM_019074.4(DLL4):c.1291G>A (p.Gly431Arg) rs1892843062
NM_019074.4(DLL4):c.1312G>A (p.Glu438Lys)
NM_019074.4(DLL4):c.1327G>A (p.Asp443Asn)
NM_019074.4(DLL4):c.1336C>T (p.Arg446Cys)
NM_019074.4(DLL4):c.1349C>T (p.Ala450Val)
NM_019074.4(DLL4):c.1357G>A (p.Gly453Ser)
NM_019074.4(DLL4):c.1387A>C (p.Met463Leu)
NM_019074.4(DLL4):c.1433G>A (p.Arg478Gln)
NM_019074.4(DLL4):c.1508_1510del (p.Thr503_Phe504delinsIle) rs1566879601
NM_019074.4(DLL4):c.1547G>A (p.Arg516His)
NM_019074.4(DLL4):c.1594G>A (p.Val532Ile)
NM_019074.4(DLL4):c.1598C>T (p.Ser533Leu)
NM_019074.4(DLL4):c.1640T>C (p.Met547Thr)
NM_019074.4(DLL4):c.1675C>T (p.Arg559Trp)
NM_019074.4(DLL4):c.1683C>G (p.Asp561Glu) rs1485634385
NM_019074.4(DLL4):c.1687G>A (p.Gly563Ser)
NM_019074.4(DLL4):c.1742_1750del (p.Pro581_Ala583del)
NM_019074.4(DLL4):c.1747G>T (p.Ala583Ser)
NM_019074.4(DLL4):c.1871G>A (p.Arg624Gln)
NM_019074.4(DLL4):c.1873G>C (p.Gly625Arg)
NM_019074.4(DLL4):c.1886G>A (p.Gly629Glu)
NM_019074.4(DLL4):c.1925C>T (p.Ala642Val)
NM_019074.4(DLL4):c.1934G>A (p.Arg645Gln)
NM_019074.4(DLL4):c.1943+3G>A
NM_019074.4(DLL4):c.1960C>T (p.Arg654Trp)
NM_019074.4(DLL4):c.1961G>A (p.Arg654Gln)
NM_019074.4(DLL4):c.2001G>C (p.Gln667His)
NM_019074.4(DLL4):c.200C>T (p.Ala67Val)
NM_019074.4(DLL4):c.2012T>C (p.Leu671Ser)
NM_019074.4(DLL4):c.205G>T (p.Val69Phe)
NM_019074.4(DLL4):c.233C>A (p.Thr78Asn)
NM_019074.4(DLL4):c.305C>A (p.Pro102His) rs1892742688
NM_019074.4(DLL4):c.336+6C>T rs1222577777
NM_019074.4(DLL4):c.35C>T (p.Ala12Val)
NM_019074.4(DLL4):c.382G>A (p.Asp128Asn) rs374022749
NM_019074.4(DLL4):c.392C>G (p.Pro131Arg)
NM_019074.4(DLL4):c.393A>G (p.Pro131=)
NM_019074.4(DLL4):c.395-5C>G
NM_019074.4(DLL4):c.430G>A (p.Ala144Thr) rs758331951
NM_019074.4(DLL4):c.470T>C (p.Leu157Ser) rs1336787203
NM_019074.4(DLL4):c.482C>G (p.Thr161Ser) rs2140369198
NM_019074.4(DLL4):c.488C>G (p.Thr163Ser) rs1265549771
NM_019074.4(DLL4):c.490C>T (p.Leu164Phe)
NM_019074.4(DLL4):c.507C>T (p.Tyr169=)
NM_019074.4(DLL4):c.595G>A (p.Val199Met)
NM_019074.4(DLL4):c.5C>T (p.Ala2Val) rs754069384
NM_019074.4(DLL4):c.628C>A (p.Pro210Thr)
NM_019074.4(DLL4):c.631G>A (p.Gly211Ser) rs2140369266
NM_019074.4(DLL4):c.647A>G (p.Tyr216Cys) rs2140369271
NM_019074.4(DLL4):c.704A>C (p.Lys235Thr)
NM_019074.4(DLL4):c.714G>T (p.Glu238Asp)
NM_019074.4(DLL4):c.754G>A (p.Glu252Lys)
NM_019074.4(DLL4):c.782A>G (p.His261Arg)
NM_019074.4(DLL4):c.875C>T (p.Ser292Phe) rs775291009
NM_019074.4(DLL4):c.895A>G (p.Thr299Ala) rs1200516571
NM_019074.4(DLL4):c.978C>T (p.Ser326=)
NM_019074.4(DLL4):c.979G>A (p.Glu327Lys) rs1228279248

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.