ClinVar Miner

List of variants in gene PTEN reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP
NM_000314.6(PTEN):c.-12A>T rs753142719
NM_000314.6(PTEN):c.1008C>T (p.Tyr336=) rs786201816
NM_000314.6(PTEN):c.1026+10A>G rs767777911
NM_000314.6(PTEN):c.1027-12T>G rs1057521732
NM_000314.6(PTEN):c.1027-17A>T rs1057520355
NM_000314.6(PTEN):c.1125T>C (p.Asp375=) rs1057524567
NM_000314.6(PTEN):c.114T>G (p.Pro38=) rs748040144
NM_000314.6(PTEN):c.1161A>G (p.Pro387=) rs1057523975
NM_000314.6(PTEN):c.1170A>G (p.Glu390=) rs1057524010
NM_000314.6(PTEN):c.1197A>G (p.Gln399=) rs374684043
NM_000314.6(PTEN):c.165-17G>C rs898943632
NM_000314.6(PTEN):c.165-7T>C rs572375431
NM_000314.6(PTEN):c.174T>C (p.Asp58=) rs769719835
NM_000314.6(PTEN):c.209+17A>G rs1057520524
NM_000314.6(PTEN):c.209+9_209+10delinsCC rs1060503841
NM_000314.6(PTEN):c.210-17T>C rs750987148
NM_000314.6(PTEN):c.210-3dupT rs1064794464
NM_000314.6(PTEN):c.210-6T>C rs1057521210
NM_000314.6(PTEN):c.210-7_210-3del5 rs587780544
NM_000314.6(PTEN):c.222A>G (p.Arg74=) rs781542973
NM_000314.6(PTEN):c.228T>C (p.Tyr76=) rs1554897866
NM_000314.6(PTEN):c.234C>A (p.Thr78=) rs35917308
NM_000314.6(PTEN):c.234C>T (p.Thr78=) rs35917308
NM_000314.6(PTEN):c.253+14T>A rs1057520635
NM_000314.6(PTEN):c.253+18_253+22delGTACT rs1554897892
NM_000314.6(PTEN):c.253+20_253+26delACTATGT rs1554897894
NM_000314.6(PTEN):c.254-6C>T rs1057520525
NM_000314.6(PTEN):c.258A>G (p.Ala86=) rs587780710
NM_000314.6(PTEN):c.261A>G (p.Gln87=) rs149772796
NM_000314.6(PTEN):c.321T>C (p.Asp107=) rs372876243
NM_000314.6(PTEN):c.369C>T (p.His123=) rs1085308045
NM_000314.6(PTEN):c.417A>G (p.Leu139=) rs1057520407
NM_000314.6(PTEN):c.444A>C (p.Ala148=) rs778663292
NM_000314.6(PTEN):c.456A>G (p.Leu152=) rs779626613
NM_000314.6(PTEN):c.48T>C (p.Tyr16=) rs587782187
NM_000314.6(PTEN):c.492+14T>A rs1057523132
NM_000314.6(PTEN):c.492+14dup rs1064793690
NM_000314.6(PTEN):c.492+16A>G rs1057522052
NM_000314.6(PTEN):c.493-13T>C rs1554900488
NM_000314.6(PTEN):c.493-19T>C rs1554900486
NM_000314.6(PTEN):c.493-4C>T rs1057522555
NM_000314.6(PTEN):c.513G>A (p.Gln171=) rs1554900546
NM_000314.6(PTEN):c.528T>C (p.Tyr176=) rs1057522285
NM_000314.6(PTEN):c.577C>T (p.Leu193=) rs772631069
NM_000314.6(PTEN):c.634+17C>T rs1057522469
NM_000314.6(PTEN):c.635-14A>G rs758742080
NM_000314.6(PTEN):c.635-18A>G rs1057520441
NM_000314.6(PTEN):c.635-6A>G rs1009588340
NM_000314.6(PTEN):c.675T>C (p.Tyr225=) rs1057520900
NM_000314.6(PTEN):c.711G>A (p.Lys237=) rs773353820
NM_000314.6(PTEN):c.720C>T (p.Tyr240=) rs190070312
NM_000314.6(PTEN):c.738G>A (p.Pro246=) rs774364894
NM_000314.6(PTEN):c.78C>A (p.Thr26=) rs786201280
NM_000314.6(PTEN):c.78C>T (p.Thr26=) rs786201280
NM_000314.6(PTEN):c.80-11A>G rs776590293
NM_000314.6(PTEN):c.801+15T>C rs1057520830
NM_000314.6(PTEN):c.801+9T>C rs1060503839
NM_000314.6(PTEN):c.802-17T>C rs1057520419
NM_000314.6(PTEN):c.802-23_802-13delCTTTTCTTTTT rs1064794381
NM_000314.6(PTEN):c.802-29_802-20delCTTTTTCTTT rs1064793331
NM_000314.6(PTEN):c.802-6T>G rs1057522284
NM_000314.6(PTEN):c.802-9T>G rs1057520354
NM_000314.6(PTEN):c.831A>G (p.Thr277=) rs376886779
NM_000314.6(PTEN):c.870A>G (p.Val290=) rs529155918
NM_000314.6(PTEN):c.885A>G (p.Leu295=) rs587780713
NM_000314.6(PTEN):c.900C>T (p.Ile300=) rs550122918
NM_000314.6(PTEN):c.93C>T (p.Asn31=) rs1170214930
NM_000314.7(PTEN):c.1027-4C>G rs587782788
NM_000314.7(PTEN):c.164+12T>C rs1057521654
NM_000314.7(PTEN):c.216T>C (p.Ala72=) rs1057520862
NM_000314.7(PTEN):c.235G>A (p.Ala79Thr) rs202004587
NM_000314.7(PTEN):c.254-17T>G rs1057520819
NM_000314.7(PTEN):c.79+7A>G rs374331677

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