Evidence Repository
The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries. [Disclaimer]
  • See Evidence submitted by expert panel for details.

Variant: NM_000314.6(PTEN):c.802-2A>T

CA000591

142423 (ClinVar)

Gene: PTEN
Condition: PTEN hamartoma tumor syndrome
Inheritance Mode: Autosomal dominant inheritance
Link to MONDO
UUID: 0b5afc39-258a-4c7d-8a60-f765e5c2eaf2
Approved on: 2017-10-18
Published on: 2018-12-10

HGVS expressions

NM_000314.6:c.802-2A>T
NM_000314.6(PTEN):c.802-2A>T
NC_000010.11:g.87960892A>T
CM000672.2:g.87960892A>T
NC_000010.10:g.89720649A>T
CM000672.1:g.89720649A>T
NC_000010.9:g.89710629A>T
NG_007466.2:g.102454A>T
NM_000314.5:c.802-2A>T
NM_001304717.2:c.1321-2A>T
NM_001304718.1:c.211-2A>T
NM_000314.7:c.802-2A>T
NM_001304717.5:c.1321-2A>T
NM_001304718.2:c.211-2A>T
ENST00000371953.7:c.802-2A>T
ENST00000472832.2:n.229-2A>T
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Pathogenic

Met criteria codes 3
PS4_Supporting PM2 PVS1

Evidence Links 0

Expert Panel

Criteria Specification Information

Criteria Specifications for this VCEP
Evidence submitted by expert panel
PTEN VCEP
PTEN c.802-2A>T (IVS7-2A>T) meets criteria to be classified as pathogenic for PTEN Hamartoma Tumor syndrome in an autosomal dominant manner using modified ACMG criteria (Mester et al. 2018; manuscript in preparation). Please see a summary of the rules and criteria codes in the “PTEN ACMG Specifications Summary” document (assertion method column). PVS1: Null variant predicted to result in nonsense-mediated decay or causing truncation/frameshift at or 5’ to c.1121 (NM_000314.4). PM2: Absent in large sequenced populations (PMID 27535533). PS4_P: Proband(s) with phenotype specificity score of 1-1.5. (Internal laboratory contributor(s), SCV000222230.9)
Met criteria codes
PS4_Supporting
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PM2
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
PVS1
No code specific comments provided, please refer to the summary above or general recommendations provided in the guideline
Curation History
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