ClinVar Miner

List of variants in gene PTEN reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_000314.8(PTEN):c.*1516T>C rs701848 0.32619
NM_000314.8(PTEN):c.*2185C>T rs11202607 0.06759
NM_000314.8(PTEN):c.*2415C>G rs34761252 0.01809
NM_000314.8(PTEN):c.*1565C>A rs34140758 0.01132
NM_000314.8(PTEN):c.*1955T>A rs41284072 0.01082
NM_000314.8(PTEN):c.*1954A>T rs35914322 0.00268
NM_000314.8(PTEN):c.-165C>G rs575260016 0.00267
NM_000314.8(PTEN):c.*2162A>G rs574993688 0.00216
NM_000314.8(PTEN):c.*2173C>T rs186996550 0.00211
NM_000314.8(PTEN):c.*1945G>A rs567800059 0.00201
NM_000314.8(PTEN):c.*1702G>A rs150265244 0.00200
NM_000314.8(PTEN):c.*353C>T rs181234898 0.00200
NM_000314.8(PTEN):c.*788T>C rs138309082 0.00200
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.*1620T>C rs568474293 0.00127
NM_000314.8(PTEN):c.-152A>G rs369849061 0.00018
NM_000314.8(PTEN):c.*1695C>A rs141857855 0.00016
NM_000314.8(PTEN):c.802-12T>C rs587781129 0.00015
NM_000314.8(PTEN):c.579G>A (p.Leu193=) rs568851024 0.00010
NM_000314.8(PTEN):c.*1237A>G rs547879223 0.00001
NM_000314.8(PTEN):c.-284C>T rs552470098
NM_000314.8(PTEN):c.-512G>A rs886047387

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