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

Minimum submission review status:		Collection method:
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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: 17

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 10q23.31(chr10:89685057-89721049)x3
NM_000314.8(PTEN):c.1026+1G>A	rs786201041
NM_000314.8(PTEN):c.1026+1G>C	rs786201041
NM_000314.8(PTEN):c.1026+1G>T	rs786201041
NM_000314.8(PTEN):c.1026+2T>G	rs1114167624
NM_000314.8(PTEN):c.1026G>A (p.Lys342=)	rs398123314
NM_000314.8(PTEN):c.1027-2A>T	rs1085308041
NM_000314.8(PTEN):c.178A>T (p.Lys60Ter)	rs1554897262
NM_000314.8(PTEN):c.210-2A>G	rs1564828914
NM_000314.8(PTEN):c.40A>G (p.Arg14Gly)	rs1085308047
NM_000314.8(PTEN):c.492+1G>A	rs1554898242
NM_000314.8(PTEN):c.493-2A>G	rs587781784
NM_000314.8(PTEN):c.635-1G>C	rs876661024
NM_000314.8(PTEN):c.635-2A>C	rs1564566706
NM_000314.8(PTEN):c.635-3C>A	rs1085308056
NM_000314.8(PTEN):c.635-3C>G	rs1085308056
NM_000314.8(PTEN):c.801+1G>T	rs786204873

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