Gene-specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel
Gene-specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel
The ClinGen PTEN Expert Panel was organized by the ClinGen Hereditary Cancer Clinical Domain Working Group to assemble clinicians, researchers, and molecular diagnosticians with PTEN expertise to develop specifications to the 2015 ACMG/AMP Sequence Variant Interpretation Guidelines for PTEN variant interpretation. We describe finalized PTEN-specific variant classification criteria and outcomes from pilot testing of 42 variants with benign/likely benign (BEN/LBEN), pathogenic/likely pathogenic (PATH/LPATH), uncertain significance (VUS), and conflicting (CONF) ClinVar assertions. Utilizing these rules, classifications concordant with ClinVar assertions were achieved for 14/15 (93.3%) BEN/LBEN and 16/16 (100%) PATH/LPATH ClinVar consensus variants for an overall concordance of 96.8% (30/31). The variant where agreement was not reached was a synonymous variant near a splice donor with noncanonical sequence for which in silico models cannot predict the native site. Applying these rules to six VUS and five CONF variants, adding shared internal laboratory data enabled one VUS to be classified as LBEN and two CONF variants to be as classified as PATH and LPATH. This study highlights the benefit of gene-specific criteria and the value of sharing internal laboratory data for variant interpretation. Our PTEN-specific criteria and expertly reviewed assertions should prove helpful for laboratories and others curating PTEN variants.
classification, ClinGen, criteria, PTEN, variant
1581-1592
Mester, Jessica L.
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Ghosh, Rajarshi
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Pesaran, Tina
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Huether, Robert
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Karam, Rachid
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Hruska, Kathleen S.
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Costa, Helio A.
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Lachlan, Katherine
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Ngeow, Joanne
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Barnholtz-Sloan, Jill
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Sesock, Kaitlin
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Hernandez, Felicia
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Zhang, Liying
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Milko, Laura
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Plon, Sharon E.
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Hegde, Madhuri
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Eng, Charis
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1 November 2018
Mester, Jessica L.
609b6e86-b7c1-4771-b632-d38320913f58
Ghosh, Rajarshi
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Pesaran, Tina
f5b30177-f11e-4c14-95fe-e23b663c5867
Huether, Robert
056ee88b-0fa3-44c9-aabc-b373c677c11f
Karam, Rachid
2a247747-3daa-44b1-aab7-7a3d27914249
Hruska, Kathleen S.
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Costa, Helio A.
e6026e16-db4e-477a-9b54-3cd99e79e0e7
Lachlan, Katherine
175ce889-ede8-477e-93eb-afefc1af5dda
Ngeow, Joanne
2b13a275-7c4b-418f-bbdf-97c4c254817a
Barnholtz-Sloan, Jill
d26ce878-5a65-4abf-9aba-0e504c51ca4d
Sesock, Kaitlin
64c2b919-1591-4766-af10-c5d5708a5439
Hernandez, Felicia
bc29d904-aa95-47b8-9f1d-f2d242621ae0
Zhang, Liying
8a0e454d-d7a9-4363-8904-d79355e11ce7
Milko, Laura
deb0732c-0b07-4902-bb2c-009d97c228bb
Plon, Sharon E.
1b20dc19-b1d5-4240-bd5c-31d7f4f285b2
Hegde, Madhuri
818c8290-9cae-4845-b199-789d12493d7a
Eng, Charis
249f0609-040a-47de-8c3c-c77d9823a230
Mester, Jessica L., Ghosh, Rajarshi, Pesaran, Tina, Huether, Robert, Karam, Rachid, Hruska, Kathleen S., Costa, Helio A., Lachlan, Katherine, Ngeow, Joanne, Barnholtz-Sloan, Jill, Sesock, Kaitlin, Hernandez, Felicia, Zhang, Liying, Milko, Laura, Plon, Sharon E., Hegde, Madhuri and Eng, Charis
(2018)
Gene-specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel.
Human Mutation, 39 (11), .
(doi:10.1002/humu.23636).
Abstract
The ClinGen PTEN Expert Panel was organized by the ClinGen Hereditary Cancer Clinical Domain Working Group to assemble clinicians, researchers, and molecular diagnosticians with PTEN expertise to develop specifications to the 2015 ACMG/AMP Sequence Variant Interpretation Guidelines for PTEN variant interpretation. We describe finalized PTEN-specific variant classification criteria and outcomes from pilot testing of 42 variants with benign/likely benign (BEN/LBEN), pathogenic/likely pathogenic (PATH/LPATH), uncertain significance (VUS), and conflicting (CONF) ClinVar assertions. Utilizing these rules, classifications concordant with ClinVar assertions were achieved for 14/15 (93.3%) BEN/LBEN and 16/16 (100%) PATH/LPATH ClinVar consensus variants for an overall concordance of 96.8% (30/31). The variant where agreement was not reached was a synonymous variant near a splice donor with noncanonical sequence for which in silico models cannot predict the native site. Applying these rules to six VUS and five CONF variants, adding shared internal laboratory data enabled one VUS to be classified as LBEN and two CONF variants to be as classified as PATH and LPATH. This study highlights the benefit of gene-specific criteria and the value of sharing internal laboratory data for variant interpretation. Our PTEN-specific criteria and expertly reviewed assertions should prove helpful for laboratories and others curating PTEN variants.
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Accepted/In Press date: 28 August 2018
e-pub ahead of print date: 11 October 2018
Published date: 1 November 2018
Keywords:
classification, ClinGen, criteria, PTEN, variant
Identifiers
Local EPrints ID: 427742
URI: http://eprints.soton.ac.uk/id/eprint/427742
ISSN: 1059-7794
PURE UUID: 99251fed-a2e0-477c-91a9-8d48ec81bfb2
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Date deposited: 25 Jan 2019 17:30
Last modified: 15 Mar 2024 22:15
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Contributors
Author:
Jessica L. Mester
Author:
Rajarshi Ghosh
Author:
Tina Pesaran
Author:
Robert Huether
Author:
Rachid Karam
Author:
Kathleen S. Hruska
Author:
Helio A. Costa
Author:
Katherine Lachlan
Author:
Joanne Ngeow
Author:
Jill Barnholtz-Sloan
Author:
Kaitlin Sesock
Author:
Felicia Hernandez
Author:
Liying Zhang
Author:
Laura Milko
Author:
Sharon E. Plon
Author:
Madhuri Hegde
Author:
Charis Eng
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