List of variants in gene PTEN reported as likely pathogenic for nervous system cancer

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.388C>T (p.Arg130Ter)	rs121909224	0.00001
NM_000314.8(PTEN):c.517C>T (p.Arg173Cys)	rs121913293	0.00001
NM_000314.8(PTEN):c.518G>A (p.Arg173His)	rs121913294	0.00001
NM_000314.8(PTEN):c.1003C>T (p.Arg335Ter)	rs121909231
NM_000314.8(PTEN):c.388C>G (p.Arg130Gly)	rs121909224
NM_000314.8(PTEN):c.389G>A (p.Arg130Gln)	rs121909229
NM_000314.8(PTEN):c.389G>C (p.Arg130Pro)	rs121909229
NM_000314.8(PTEN):c.389G>T (p.Arg130Leu)	rs121909229
NM_000314.8(PTEN):c.698G>A (p.Arg233Gln)	rs770025422

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