ClinVar Miner

List of variants in gene PTEN reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_000314.8(PTEN):c.-326G>C rs2943772 0.99984
NC_000010.11:g.87864104del rs71022512 0.99907
NM_000314.8(PTEN):c.1026+219C>T rs2736627 0.92008
NM_000314.8(PTEN):c.1026+32T>G rs555895 0.40232
NM_000314.8(PTEN):c.80-96A>G rs1903858 0.38960
NM_000314.8(PTEN):c.254-316T>C rs34973022 0.02173
NM_000314.8(PTEN):c.802-207T>C rs147038309 0.02001
NM_000314.8(PTEN):c.492+217C>T rs35560700 0.01599
NM_000314.8(PTEN):c.492+292T>C rs34826144 0.01411
NM_000314.8(PTEN):c.*1499C>T rs180953647 0.00272
NM_000314.8(PTEN):c.209+84G>A rs185262832 0.00199
NM_000314.8(PTEN):c.210-39A>G rs370918174 0.00177
NM_000314.8(PTEN):c.132C>T (p.Gly44=) rs150651961 0.00168
NM_000314.8(PTEN):c.634+136G>A rs149607752 0.00165
NM_000314.8(PTEN):c.1104T>C (p.Asp368=) rs35979531 0.00158
NM_000314.8(PTEN):c.-9C>G rs11202592 0.00139
NM_000314.8(PTEN):c.79+35C>T rs190707033 0.00130
NM_000314.8(PTEN):c.*1583G>A rs548599209 0.00112
NM_000314.8(PTEN):c.234C>T (p.Thr78=) rs35917308 0.00016
NM_000314.8(PTEN):c.254-37T>C rs767612524 0.00003
NM_000314.8(PTEN):c.635-16G>A rs750772657 0.00003
NM_000314.8(PTEN):c.801+18A>T rs777679092 0.00003
NM_000314.8(PTEN):c.411A>G (p.Ala137=) rs144545031 0.00002
NM_000314.8(PTEN):c.288A>G (p.Pro96=) rs746661067 0.00001
NM_000314.8(PTEN):c.321T>C (p.Asp107=) rs372876243 0.00001
NM_000314.8(PTEN):c.78C>T (p.Thr26=) rs786201280 0.00001
GRCh37/hg19 10q23.31(chr10:89624218-89657150)x3
GRCh37/hg19 10q23.31(chr10:89624218-89726873)x3
GRCh37/hg19 10q23.31(chr10:89624218-89741806)x3
GRCh37/hg19 10q23.31(chr10:89624218-89778495)x3
GRCh37/hg19 10q23.31(chr10:89624218-89782386)x3
GRCh37/hg19 10q23.31(chr10:89624413-89657150)x3
GRCh37/hg19 10q23.31(chr10:89624413-89657594)x3
GRCh37/hg19 10q23.31(chr10:89624413-89726873)x3
GRCh37/hg19 10q23.31(chr10:89624413-89779324)x3
GRCh37/hg19 10q23.31(chr10:89624422-89655408)x3
GRCh37/hg19 10q23.31(chr10:89625234-89657150)x3
GRCh37/hg19 10q23.31(chr10:89625234-89657594)x3
GRCh37/hg19 10q23.31(chr10:89625582-89657150)x3
GRCh37/hg19 10q23.31(chr10:89625582-89782386)x3
GRCh37/hg19 10q23.31(chr10:89626086-89657150)x3
GRCh37/hg19 10q23.31(chr10:89649838-89653686)x1
GRCh37/hg19 10q23.31(chr10:89652878-89653686)x1
GRCh37/hg19 10q23.31(chr10:89652878-89657150)x1
GRCh37/hg19 10q23.31(chr10:89664047-89727414)x3
GRCh37/hg19 10q23.31(chr10:89664047-89745814)x3
GRCh37/hg19 10q23.31(chr10:89664047-89778495)x3
GRCh37/hg19 10q23.31(chr10:89678296-89722446)x3
GRCh37/hg19 10q23.31(chr10:89678296-89782386)x3
GRCh37/hg19 10q23.31(chr10:89688549-89745814)x3
GRCh37/hg19 10q23.31(chr10:89689267-89697353)x1
GRCh37/hg19 10q23.31(chr10:89689267-89698190)x1
GRCh37/hg19 10q23.31(chr10:89689267-89722446)x3
GRCh37/hg19 10q23.31(chr10:89689282-89696588)x1
GRCh37/hg19 10q23.31(chr10:89689282-89698190)x1
GRCh37/hg19 10q23.31(chr10:89689391-89695370)x1
NM_000314.8(PTEN):c.*10dup rs756681683
NM_000314.8(PTEN):c.*1447_*1459del
NM_000314.8(PTEN):c.-284C>T rs552470098
NM_000314.8(PTEN):c.-511G>A rs12573787
NM_000314.8(PTEN):c.-513G>C rs546504608
NM_000314.8(PTEN):c.1026+20T>G rs753190893
NM_000314.8(PTEN):c.165-24TTTG[2] rs786204877
NM_000314.8(PTEN):c.209+76A>C rs2132232633
NM_000314.8(PTEN):c.210-7_210-3del rs587780544
NM_000314.8(PTEN):c.253+109_253+110insTCTTA rs1799734
NM_000314.8(PTEN):c.493-12dup rs756623620
NM_000314.8(PTEN):c.802-3dup rs34003473
NM_000314.8(PTEN):c.802-51_802-14del rs557364463

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