ClinVar Miner

List of variants in gene PTEN reported as benign

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
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(chr10:89685136-89685328)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
NC_000010.10:g.(?_89720598)_(89720635_?)del38
NM_000314.6(PTEN):c.-1027C>A rs587781128
NM_000314.6(PTEN):c.-903G>A rs1044322
NM_000314.6(PTEN):c.-975G>A rs587780001
NM_000314.6(PTEN):c.165-13_165-10delGTTT rs786204877
NM_000314.6(PTEN):c.802-18_802-14delCTTTT rs786204879
NM_000314.6(PTEN):c.802-3dupT rs34003473
NM_000314.6(PTEN):c.802-4_802-3dupTT rs34003473
NM_000314.7(PTEN):c.*10del rs756681683
NM_000314.7(PTEN):c.*1516T>C rs701848
NM_000314.7(PTEN):c.*2185C>T rs11202607
NM_000314.7(PTEN):c.*75del rs878853930
NM_000314.7(PTEN):c.-326= rs2943772
NM_000314.7(PTEN):c.-366del rs1554890188
NM_000314.7(PTEN):c.-511G>A rs886047387
NM_000314.7(PTEN):c.-545_-543GGC[6] rs34413673
NM_000314.7(PTEN):c.-662_-651del rs786204880
NM_000314.7(PTEN):c.-975G>C rs587780001
NM_000314.7(PTEN):c.-9C>G rs11202592
NM_000314.7(PTEN):c.1026+32T>G rs555895
NM_000314.7(PTEN):c.1104T>C (p.Asp368=) rs35979531
NM_000314.7(PTEN):c.132C>T (p.Gly44=) rs150651961
NM_000314.7(PTEN):c.210-39A>G rs370918174
NM_000314.7(PTEN):c.210-48_210-44del rs765853588
NM_000314.7(PTEN):c.210-7_210-3del rs587780544
NM_000314.7(PTEN):c.210-9T>C rs751744545
NM_000314.7(PTEN):c.253+66A>G rs377719086
NM_000314.7(PTEN):c.254-30dup rs77494260
NM_000314.7(PTEN):c.254-316T>C
NM_000314.7(PTEN):c.321T>C (p.Asp107=) rs372876243
NM_000314.7(PTEN):c.360A>C (p.Ala120=) rs759485888
NM_000314.7(PTEN):c.492+14dup rs1064793690
NM_000314.7(PTEN):c.492+217C>T
NM_000314.7(PTEN):c.492+292T>C
NM_000314.7(PTEN):c.579G>A (p.Leu193=) rs568851024
NM_000314.7(PTEN):c.651C>T (p.Val217=) rs886038278
NM_000314.7(PTEN):c.78C>T (p.Thr26=) rs786201280
NM_000314.7(PTEN):c.79+35C>T rs190707033
NM_000314.7(PTEN):c.80-96A>G rs1903858
NM_000314.7(PTEN):c.802-12T>C rs587781129
NM_000314.7(PTEN):c.802-18C>T rs376702513
NM_000314.7(PTEN):c.802-207T>C
NM_000314.7(PTEN):c.802-3del rs34003473
NM_000314.7(PTEN):c.802-51_802-14del rs557364463
NM_000314.7(PTEN):c.804C>A (p.Asp268Glu) rs398123328
NM_000314.7(PTEN):c.855A>G (p.Glu285=) rs751888926
NM_000314.7(PTEN):c.960A>G (p.Leu320=) rs886038279
NM_001126049.1(KLLN):c.-956G>T rs34149102
Single allele rs71022512

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