ClinVar Miner

List of variants in gene PTEN reported as likely benign for Hereditary cancer-predisposing syndrome

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 214
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HGVS dbSNP
NM_000314.4(PTEN):c.1104T>C (p.Asp368=) rs35979531
NM_000314.6(PTEN):c.*10T>A rs769236743
NM_000314.6(PTEN):c.*10delT rs756681683
NM_000314.6(PTEN):c.*10dup rs756681683
NM_000314.6(PTEN):c.-14A>C rs755295390
NM_000314.6(PTEN):c.1005A>G (p.Arg335=) rs1303065649
NM_000314.6(PTEN):c.1008C>T (p.Tyr336=) rs786201816
NM_000314.6(PTEN):c.1011T>C (p.Phe337=) rs876659916
NM_000314.6(PTEN):c.1017A>G (p.Pro339=) rs1554825644
NM_000314.6(PTEN):c.1026+10A>G rs767777911
NM_000314.6(PTEN):c.1026+111T>C rs766288989
NM_000314.6(PTEN):c.1026+121C>T rs536465299
NM_000314.6(PTEN):c.1026+20T>G rs753190893
NM_000314.6(PTEN):c.1027-6C>T rs1374474745
NM_000314.6(PTEN):c.1029G>A (p.Val343=) rs1393550059
NM_000314.6(PTEN):c.1050A>G (p.Thr350=) rs769324650
NM_000314.6(PTEN):c.1062G>A (p.Pro354=) rs786202751
NM_000314.6(PTEN):c.1092T>C (p.Ser364=) rs1355576298
NM_000314.6(PTEN):c.1098A>C (p.Thr366=) rs1554826045
NM_000314.6(PTEN):c.1107T>C (p.Val369=) rs1554826048
NM_000314.6(PTEN):c.1131T>C (p.Tyr377=) rs1345063638
NM_000314.6(PTEN):c.1134A>G (p.Arg378=) rs1554826056
NM_000314.6(PTEN):c.1137T>C (p.Tyr379=) rs1295420243
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.1173T>G (p.Pro391=) rs1554826062
NM_000314.6(PTEN):c.1188G>A (p.Gln396=) rs786202062
NM_000314.6(PTEN):c.1197A>G (p.Gln399=) rs374684043
NM_000314.6(PTEN):c.1203A>G (p.Thr401=) rs876659102
NM_000314.6(PTEN):c.132C>T (p.Gly44=) rs150651961
NM_000314.6(PTEN):c.144C>T (p.Asn48=) rs762518389
NM_000314.6(PTEN):c.159A>G (p.Val53=) rs189583426
NM_000314.6(PTEN):c.164+324G>A rs181780682
NM_000314.6(PTEN):c.164+4A>G rs1554893837
NM_000314.6(PTEN):c.165-10233G>A rs368333033
NM_000314.6(PTEN):c.165-10234C>T rs111627758
NM_000314.6(PTEN):c.165-17G>C rs898943632
NM_000314.6(PTEN):c.165-4T>C rs1554897247
NM_000314.6(PTEN):c.165-7T>C rs572375431
NM_000314.6(PTEN):c.165-8_165-4delGTTTT rs760571273
NM_000314.6(PTEN):c.165-9280G>A rs869312639
NM_000314.6(PTEN):c.165-9285G>A rs758151355
NM_000314.6(PTEN):c.174T>C (p.Asp58=) rs769719835
NM_000314.6(PTEN):c.180G>A (p.Lys60=) rs972166984
NM_000314.6(PTEN):c.183T>C (p.His61=) rs876659980
NM_000314.6(PTEN):c.18A>G (p.Lys6=) rs876660391
NM_000314.6(PTEN):c.195C>T (p.Tyr65=) rs878853936
NM_000314.6(PTEN):c.204C>T (p.Tyr68=) rs773176120
NM_000314.6(PTEN):c.209+2046C>T rs869312633
NM_000314.6(PTEN):c.209+239A>G rs754041126
NM_000314.6(PTEN):c.209+736A>G rs869312643
NM_000314.6(PTEN):c.209+769T>C rs34382179
NM_000314.6(PTEN):c.209+7A>T rs1554897284
NM_000314.6(PTEN):c.209+9_209+10delinsCC rs1060503841
NM_000314.6(PTEN):c.210-17T>C rs750987148
NM_000314.6(PTEN):c.210-2616C>T rs869312631
NM_000314.6(PTEN):c.210-39A>G rs370918174
NM_000314.6(PTEN):c.210-7_210-3del5 rs587780544
NM_000314.6(PTEN):c.210-9T>C rs751744545
NM_000314.6(PTEN):c.222A>G (p.Arg74=) rs781542973
NM_000314.6(PTEN):c.231C>T (p.Asp77=) rs755953294
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.254-38delT rs77494260
NM_000314.6(PTEN):c.254-39G>T rs35034871
NM_000314.6(PTEN):c.254-40A>G rs767049245
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.264T>C (p.Tyr88=) rs1554898056
NM_000314.6(PTEN):c.288A>G (p.Pro96=) rs746661067
NM_000314.6(PTEN):c.321T>C (p.Asp107=) rs372876243
NM_000314.6(PTEN):c.330A>G (p.Gln110=) rs786201929
NM_000314.6(PTEN):c.348C>T (p.Asp116=) rs1114167651
NM_000314.6(PTEN):c.357T>G (p.Val119=) rs1554898115
NM_000314.6(PTEN):c.360A>C (p.Ala120=) rs759485888
NM_000314.6(PTEN):c.411A>G (p.Ala137=) rs144545031
NM_000314.6(PTEN):c.426G>C (p.Arg142=) rs878853939
NM_000314.6(PTEN):c.447A>G (p.Gln149=) rs750401982
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+14dup rs1064793690
NM_000314.6(PTEN):c.492+57A>G rs768719539
NM_000314.6(PTEN):c.492+5832A>G rs7896192
NM_000314.6(PTEN):c.492+5850T>A rs869312637
NM_000314.6(PTEN):c.493-12dup rs756623620
NM_000314.6(PTEN):c.493-2809A>G rs575960288
NM_000314.6(PTEN):c.493-7489A>G rs76052269
NM_000314.6(PTEN):c.493-889G>A rs531033912
NM_000314.6(PTEN):c.522T>C (p.Tyr174=) rs786201867
NM_000314.6(PTEN):c.528T>C (p.Tyr176=) rs1057522285
NM_000314.6(PTEN):c.534T>C (p.Tyr178=) rs104894184
NM_000314.6(PTEN):c.54G>A (p.Glu18=) rs1554890388
NM_000314.6(PTEN):c.573G>A (p.Val191=) rs374478092
NM_000314.6(PTEN):c.577C>T (p.Leu193=) rs772631069
NM_000314.6(PTEN):c.579G>A (p.Leu193=) rs568851024
NM_000314.6(PTEN):c.579G>C (p.Leu193=) rs568851024
NM_000314.6(PTEN):c.579G>T (p.Leu193=) rs568851024
NM_000314.6(PTEN):c.585T>C (p.Phe195=) rs1554900624
NM_000314.6(PTEN):c.618C>T (p.Phe206=) rs786202773
NM_000314.6(PTEN):c.624C>T (p.Gly208=) rs370162160
NM_000314.6(PTEN):c.634+645G>A rs543066886
NM_000314.6(PTEN):c.635-14A>G rs758742080
NM_000314.6(PTEN):c.635-19T>C rs1554825144
NM_000314.6(PTEN):c.635-696G>C rs34513359
NM_000314.6(PTEN):c.66C>T (p.Asp22=) rs786201335
NM_000314.6(PTEN):c.687A>G (p.Ser229=) rs1554825185
NM_000314.6(PTEN):c.697C>A (p.Arg233=) rs121909219
NM_000314.6(PTEN):c.720C>T (p.Tyr240=) rs190070312
NM_000314.6(PTEN):c.723T>C (p.Phe241=) rs17849090
NM_000314.6(PTEN):c.726G>A (p.Glu242=) rs1554825212
NM_000314.6(PTEN):c.738G>A (p.Pro246=) rs774364894
NM_000314.6(PTEN):c.750T>C (p.Cys250=) rs767623493
NM_000314.6(PTEN):c.759C>T (p.Ile253=) rs752250585
NM_000314.6(PTEN):c.75G>A (p.Leu25=) rs786201506
NM_000314.6(PTEN):c.768G>A (p.Glu256=) rs1554825244
NM_000314.6(PTEN):c.780A>G (p.Lys260=) rs876658720
NM_000314.6(PTEN):c.783G>A (p.Gln261=) rs760146269
NM_000314.6(PTEN):c.78C>T (p.Thr26=) rs786201280
NM_000314.6(PTEN):c.79+10657T>C rs34248932
NM_000314.6(PTEN):c.79+10771G>T rs869312634
NM_000314.6(PTEN):c.79+10772A>G rs869312632
NM_000314.6(PTEN):c.79+11548A>G rs566066891
NM_000314.6(PTEN):c.79+11557A>C rs531847666
NM_000314.6(PTEN):c.79+11873T>C rs869312636
NM_000314.6(PTEN):c.79+11891T>C rs869312635
NM_000314.6(PTEN):c.79+12219A>G rs774019645
NM_000314.6(PTEN):c.79+13451A>C rs187125801
NM_000314.6(PTEN):c.79+1409T>C rs869312638
NM_000314.6(PTEN):c.79+14412A>G rs148088027
NM_000314.6(PTEN):c.79+14637T>C rs557466351
NM_000314.6(PTEN):c.79+16G>C rs768604051
NM_000314.6(PTEN):c.79+2379G>A rs869312642
NM_000314.6(PTEN):c.79+23_79+25delCTC rs1221062997
NM_000314.6(PTEN):c.79+3193A>G rs189221275
NM_000314.6(PTEN):c.79+31_79+34delCTTT rs1465716096
NM_000314.6(PTEN):c.79+35C>T rs190707033
NM_000314.6(PTEN):c.79+369G>A rs748130964
NM_000314.6(PTEN):c.79+376T>A rs568732002
NM_000314.6(PTEN):c.79+436C>T rs34370865
NM_000314.6(PTEN):c.79+4399C>T rs869312645
NM_000314.6(PTEN):c.79+452C>T rs117587034
NM_000314.6(PTEN):c.79+968A>G rs869312646
NM_000314.6(PTEN):c.79+9762G>A rs869312640
NM_000314.6(PTEN):c.795A>C (p.Leu265=) rs891648600
NM_000314.6(PTEN):c.795A>G (p.Leu265=) rs891648600
NM_000314.6(PTEN):c.80-11414T>C rs114277912
NM_000314.6(PTEN):c.80-11759G>A rs79835941
NM_000314.6(PTEN):c.80-11A>G rs776590293
NM_000314.6(PTEN):c.80-12951T>C rs142080608
NM_000314.6(PTEN):c.80-14058G>C rs182725594
NM_000314.6(PTEN):c.80-14A>T rs768354874
NM_000314.6(PTEN):c.80-19C>A rs1554893737
NM_000314.6(PTEN):c.801+1187A>G rs869312641
NM_000314.6(PTEN):c.801+15T>C rs1057520830
NM_000314.6(PTEN):c.801+281A>G rs559574747
NM_000314.6(PTEN):c.801+9T>C rs1060503839
NM_000314.6(PTEN):c.802-2dup rs1554825500
NM_000314.6(PTEN):c.802-3delT rs34003473
NM_000314.6(PTEN):c.802-4_802-3delTT rs34003473
NM_000314.6(PTEN):c.802-4_802-3dupTT rs34003473
NM_000314.6(PTEN):c.802-558T>C rs869312644
NM_000314.6(PTEN):c.802-5_802-3delTTT rs34003473
NM_000314.6(PTEN):c.819T>C (p.Phe273=) rs876658729
NM_000314.6(PTEN):c.828T>C (p.Asn276=) rs1554825510
NM_000314.6(PTEN):c.831A>G (p.Thr277=) rs376886779
NM_000314.6(PTEN):c.843A>G (p.Pro281=) rs1554825518
NM_000314.6(PTEN):c.855A>G (p.Glu285=) rs751888926
NM_000314.6(PTEN):c.858C>G (p.Thr286=) rs876660443
NM_000314.6(PTEN):c.870A>G (p.Val290=) rs529155918
NM_000314.6(PTEN):c.882T>G (p.Ser294Arg) rs143335584
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.909T>A (p.Ile303=) rs878853945
NM_000314.6(PTEN):c.939G>A (p.Lys313=) rs562164491
NM_000314.6(PTEN):c.93C>T (p.Asn31=) rs1170214930
NM_000314.6(PTEN):c.948A>G (p.Leu316=) rs775997892
NM_000314.6(PTEN):c.951A>C (p.Val317=) rs876659993
NM_000314.6(PTEN):c.99T>C (p.Ile33=) rs786201650
NM_000314.6(PTEN):c.9C>T (p.Ala3=) rs1554890328
NM_000314.7(PTEN):c.*1A>T
NM_000314.7(PTEN):c.*5T>C rs1006891299
NM_000314.7(PTEN):c.-10G>A
NM_000314.7(PTEN):c.-798G>C rs587779992
NM_000314.7(PTEN):c.-909T>C rs550385924
NM_000314.7(PTEN):c.1026+11_1026+15del
NM_000314.7(PTEN):c.1035G>A (p.Leu345=)
NM_000314.7(PTEN):c.164+12T>C rs1057521654
NM_000314.7(PTEN):c.213T>C (p.Cys71=)
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.254-39G>A
NM_000314.7(PTEN):c.291G>A (p.Gln97=)
NM_000314.7(PTEN):c.294A>G (p.Leu98=) rs770224289
NM_000314.7(PTEN):c.33A>G (p.Arg11=)
NM_000314.7(PTEN):c.366T>C (p.Ile122=)
NM_000314.7(PTEN):c.408T>C (p.Cys136=)
NM_000314.7(PTEN):c.441G>A (p.Lys147=)
NM_000314.7(PTEN):c.493-14T>C
NM_000314.7(PTEN):c.634+14A>T
NM_000314.7(PTEN):c.693C>T (p.Pro231=) rs1064795327
NM_000314.7(PTEN):c.79+11C>T
NM_000314.7(PTEN):c.79+20C>G rs587781291
NM_000314.7(PTEN):c.80-18C>G
NM_000314.7(PTEN):c.80-8G>A
NM_000314.7(PTEN):c.801+14T>C
NM_000314.7(PTEN):c.801+18A>T
NM_000314.7(PTEN):c.801+8C>G rs1057517630
NM_000314.7(PTEN):c.816C>T (p.His272=) rs876659761
NM_000314.7(PTEN):c.861A>G (p.Ser287=)
NM_000314.7(PTEN):c.882T>C (p.Ser294=)
NM_000314.7(PTEN):c.966A>G (p.Lys322=) rs786201392

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