ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_000314.6(PTEN):c.-1027C>A rs587781128
NM_000314.7(PTEN):c.*1131del rs547262170
NM_000314.7(PTEN):c.*1237A>G rs547879223
NM_000314.7(PTEN):c.*1499C>T rs180953647
NM_000314.7(PTEN):c.*1565C>A rs34140758
NM_000314.7(PTEN):c.*1620T>C rs568474293
NM_000314.7(PTEN):c.*1702G>A rs150265244
NM_000314.7(PTEN):c.*1745G>A rs116248217
NM_000314.7(PTEN):c.*1945G>A rs567800059
NM_000314.7(PTEN):c.*1954A>T rs35914322
NM_000314.7(PTEN):c.*1955T>A rs41284072
NM_000314.7(PTEN):c.*2162A>G rs574993688
NM_000314.7(PTEN):c.*2173C>T rs186996550
NM_000314.7(PTEN):c.*2204T>A rs552431817
NM_000314.7(PTEN):c.*2415C>G rs34761252
NM_000314.7(PTEN):c.*2551G>A rs537283839
NM_000314.7(PTEN):c.*282G>A rs576872432
NM_000314.7(PTEN):c.*353C>T rs181234898
NM_000314.7(PTEN):c.*421T>C rs141648241
NM_000314.7(PTEN):c.*601A>G rs371547288
NM_000314.7(PTEN):c.*666dup rs543873570
NM_000314.7(PTEN):c.*788T>C rs138309082
NM_000314.7(PTEN):c.-152A>G rs369849061
NM_000314.7(PTEN):c.-165C>G rs575260016
NM_000314.7(PTEN):c.-284C>T rs552470098
NM_000314.7(PTEN):c.-533G>T rs886047385
NM_000314.7(PTEN):c.-674C>T rs876661258
NM_000314.7(PTEN):c.-9C>G rs11202592
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.234C>T (p.Thr78=) rs35917308
NM_000314.7(PTEN):c.579G>A (p.Leu193=) rs568851024

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