ClinVar Miner

List of variants in gene ZEB2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_014795.4(ZEB2):c.489C>T (p.Ile163=) rs138859323 0.00277
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser) rs144952836 0.00206
NM_014795.4(ZEB2):c.3471C>T (p.Asp1157=) rs149526010 0.00186
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val) rs112005830 0.00087
NM_014795.4(ZEB2):c.2206A>G (p.Met736Val) rs139191491 0.00067
NM_014795.4(ZEB2):c.2205T>C (p.Pro735=) rs149964599 0.00062
NM_014795.4(ZEB2):c.1306A>G (p.Met436Val) rs145812868 0.00052
NM_014795.4(ZEB2):c.1438G>T (p.Ala480Ser) rs143854197 0.00026
NM_014795.4(ZEB2):c.462G>A (p.Glu154=) rs372940559 0.00023
NM_014795.4(ZEB2):c.3057C>T (p.Tyr1019=) rs541915540 0.00016
NM_014795.4(ZEB2):c.10C>G (p.Pro4Ala) rs146394306 0.00015
NM_014795.4(ZEB2):c.395A>G (p.Asn132Ser) rs369622877 0.00004
NM_014795.4(ZEB2):c.2255C>T (p.Thr752Met) rs143438888 0.00003
NM_014795.4(ZEB2):c.2215A>G (p.Ile739Val) rs730881178 0.00002
NM_014795.4(ZEB2):c.2342A>G (p.Asn781Ser) rs750936389 0.00002
NM_014795.4(ZEB2):c.2946C>T (p.Ser982=) rs769095107 0.00002
NM_014795.4(ZEB2):c.97G>A (p.Asp33Asn) rs1460150528 0.00002
NM_014795.4(ZEB2):c.2256G>A (p.Thr752=) rs772121083 0.00001
NM_014795.4(ZEB2):c.2325G>A (p.Leu775=) rs1553961560 0.00001
NM_014795.4(ZEB2):c.2935A>G (p.Met979Val) rs777220598 0.00001
NM_014795.4(ZEB2):c.1146_1150del (p.Glu383fs)
NM_014795.4(ZEB2):c.1220A>G (p.His407Arg)
NM_014795.4(ZEB2):c.1257del (p.Gly421fs) rs786204801
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=) rs34890427
NM_014795.4(ZEB2):c.1447A>G (p.Ile483Val)
NM_014795.4(ZEB2):c.1516_1518del (p.Pro506del) rs1276023381
NM_014795.4(ZEB2):c.1542G>T (p.Pro514=) rs141674976
NM_014795.4(ZEB2):c.1557del (p.Asn519fs)
NM_014795.4(ZEB2):c.1648C>T (p.Gln550Ter)
NM_014795.4(ZEB2):c.1658A>T (p.Asn553Ile)
NM_014795.4(ZEB2):c.2140C>A (p.Pro714Thr)
NM_014795.4(ZEB2):c.2538T>A (p.His846Gln) rs557767273
NM_014795.4(ZEB2):c.2547T>G (p.Val849=) rs908943407
NM_014795.4(ZEB2):c.2644C>T (p.Pro882Ser)
NM_014795.4(ZEB2):c.2752C>T (p.Pro918Ser) rs1560605894
NM_014795.4(ZEB2):c.2774G>C (p.Gly925Ala)
NM_014795.4(ZEB2):c.2887-5C>T
NM_014795.4(ZEB2):c.2926C>T (p.Leu976=)
NM_014795.4(ZEB2):c.3031del (p.Ser1011fs)
NM_014795.4(ZEB2):c.377T>C (p.Ile126Thr)

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