List of variants in gene PTEN reported as uncertain significance for familial multiple meningioma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.882T>G (p.Ser294Arg)	rs143335584	0.00029
NM_000314.8(PTEN):c.892C>G (p.Gln298Glu)	rs371387815	0.00009
NM_000314.8(PTEN):c.-121A>G	rs886047395	0.00004
NM_000314.8(PTEN):c.1061C>A (p.Pro354Gln)	rs375709098	0.00003
NM_000314.8(PTEN):c.-765G>A	rs587776674	0.00002
NM_000314.8(PTEN):c.-752G>A	rs1256922808
NM_000314.8(PTEN):c.-752GGC[4]	rs933847861
NM_000314.8(PTEN):c.1189C>T (p.His397Tyr)	rs1589669413
NM_000314.8(PTEN):c.166T>A (p.Phe56Ile)	rs1589640376
NM_000314.8(PTEN):c.488A>G (p.Lys163Arg)	rs786202753
NM_000314.8(PTEN):c.593T>C (p.Met198Thr)	rs1554900635
NM_000314.8(PTEN):c.734A>C (p.Gln245Pro)	rs1057518538
NM_000314.8(PTEN):c.862G>A (p.Glu288Lys)	rs1554825528
NM_000314.8(PTEN):c.914G>A (p.Ser305Asn)	rs587780007
NM_000314.8(PTEN):c.922C>T (p.Arg308Cys)	rs1064794436

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