ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 42
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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(chr10:89688549-89745814)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_000314.6(PTEN):c.-903G>A rs1044322
NM_000314.6(PTEN):c.-975G>A rs587780001
NM_000314.6(PTEN):c.165-13_165-10delGTTT rs786204877
NM_000314.7(PTEN):c.-975G>C rs587780001
NM_000314.7(PTEN):c.132C>T (p.Gly44=) rs150651961
NM_000314.7(PTEN):c.210-39A>G rs370918174
NM_000314.7(PTEN):c.254-316T>C
NM_000314.7(PTEN):c.321T>C (p.Asp107=) rs372876243
NM_000314.7(PTEN):c.492+217C>T
NM_000314.7(PTEN):c.492+292T>C
NM_000314.7(PTEN):c.78C>T (p.Thr26=) rs786201280
NM_000314.7(PTEN):c.802-207T>C

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