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.1052_1054delTAG (p.Val351del)
- Curation Version - 1.0
- Curation History
- JSON LD for Version 1.0
CA000271
127687 (ClinVar)
Gene: PTEN
Condition: PTEN hamartoma tumor syndrome
Inheritance Mode: Autosomal dominant inheritance
UUID: ba4a2bab-161e-445b-a38c-7ef4639e08a9
Approved on: 2020-03-23
Published on: 2020-03-26
HGVS expressions
NM_000314.6:c.1052_1054delTAG
NM_000314.6(PTEN):c.1052_1054delTAG (p.Val351del)
NC_000010.11:g.87965312_87965314del
CM000672.2:g.87965312_87965314del
NC_000010.10:g.89725069_89725071del
CM000672.1:g.89725069_89725071del
NC_000010.9:g.89715049_89715051del
NG_007466.2:g.106874_106876del
NM_000314.5:c.1052_1054del
NM_000314.6:c.1052_1054del
NM_001304717.2:c.1571_1573del
NM_001304718.1:c.461_463del
NM_000314.7:c.1052_1054del
NM_001304717.5:c.1571_1573del
NM_001304718.2:c.461_463del
NM_000314.8:c.1052_1054del
ENST00000371953.7:c.1052_1054del
More
Evidence submitted by expert panel
The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. If you have questions about the information contained on this website, please see a health care professional.