The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
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- See Evidence submitted by expert panel for details.
Variant: NM_000314.6(PTEN):c.1026+1G>A
CA000103
183722 (ClinVar)
Gene: PTEN
Condition: PTEN hamartoma tumor syndrome
Inheritance Mode: Autosomal dominant inheritance
UUID: 9a0535ed-2b90-4309-917f-cbcce2549f2a
Approved on: 2017-10-18
Published on: 2018-12-10
HGVS expressions
NM_000314.6:c.1026+1G>A
NM_000314.6(PTEN):c.1026+1G>A
NM_000314.5:c.1026+1G>A
NM_001304717.2:c.1545+1G>A
NM_001304718.1:c.435+1G>A
NM_000314.7:c.1026+1G>A
NM_001304717.5:c.1545+1G>A
NM_001304718.2:c.435+1G>A
ENST00000371953.7:c.1026+1G>A
ENST00000472832.2:n.454G>A
NC_000010.11:g.87961119G>A
CM000672.2:g.87961119G>A
NC_000010.10:g.89720876G>A
CM000672.1:g.89720876G>A
NC_000010.9:g.89710856G>A
NG_007466.2:g.102681G>A
Evidence submitted by expert panel
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