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Classification of variants of reduced penetrance in high-penetrance cancer susceptibility genes: Framework for genetics clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group-UK)
Authors :
Garrett, Alice Allen, Sophie Durkie, Miranda Burghel, George J. Robinson, Rachel Callaway, Alison Field, Joanne Frugtniet, Bethan Palmer-Smith, Sheila Grant, Jonathan Pagan, Judith McDevitt, Trudi Rowlands, Charlie F. McVeigh, Terri Hanson, Helen Turnbull, Clare Turnbull, C. Garrett, A. Loong, L. Choi, S. Torr, B. Allen, S. Durkie, M. Callaway, A. Drummond, J. Burghel, G.J. Robinson, R. Berry, I.R. Wallace, A.J. Eccles, D.M. Tischkowitz, M. Ellard, S. Hanson, H. Baple, E. Evans, D.G. Woodward, E. Lalloo, F. Samant, S. Lucassen, A. Znaczko, A. Shaw, A. Ansari, A. Kumar, A. Donaldson, A. Murray, A. Ross, A. Taylor-Beadling, A. Taylor, A. Innes, A. Brady, A. Kulkarni, A. Hogg, A.C. Bowden, A. Ramsay Hadonou, A. Coad, B. McIldowie, B. Speight, B. DeSouza, B. Mullaney, B. McKenna, C. Brewer, C. Olimpio, C. Clabby, C. Crosby, C. Jenkins, C. Armstrong, C. Bowles, C. Brooks, C. Byrne, C. Maurer, C. Baralle, D. Chubb, D. Stobo, D. Moore, D. O'Sullivan, D. Donnelly, D. Randhawa, D. Halliday, D. Atkinson, E. Rauter, E. Johnston, E. Maher, E. Sofianopoulou, E. Petrides, E. McRonald, F. Pelz, F. Frayling, I. Corbett, G. Rea, G. Clouston, H. Powell, H. Williamson, H. Carley, H. Thomas, H.J.W. Tomlinson, I. Cook, J. Hoyle, J. Tellez, J. Whitworth, J. Williams, J. Murray, J. Campbell, J. Tolmie, J. Field, J. Mason, J. Burn, J. Bruty, J. Callaway, J. Grant, J. Del Rey Jimenez, J. Pagan, J. VanCampen, J. Barwell, J. Monahan, K. Tatton-Brown, K. Ong, K.R. Murphy, K. Andrews, K. Mokretar, K. Cadoo, K. Smith, K. Baker, K. Brown, K. Reay, K. McKay Bounford, K. Bradshaw, K. Russell, K. Stone, K. Snape, K. Crookes, L. Reed, L. Taggart, L. Yarram, L. Cobbold, L. Walker, L. Walker, L. Hawkes, L. Busby, L. Izatt, L. Kiely, L. Hughes, L. Side, L. Sarkies, L. Greenhalgh, K.-L. Shanmugasundaram, M. Duff, M. Bartlett, M. Watson, M. Owens, M. Bradford, M. Huxley, M. Slean, M. Ryten, M. Smith, M. Ahmed, M. Roberts, N. O'Brien, C. Middleton, O. Tarpey, P. Logan, P. Dean, P. May, P. Brace, P. Tredwell, R. Harrison, R. Hart, R. Kirk, R. Martin, R. Nyanhete, R. Wright, R. Martin, R. Davidson, R. Cleaver, R. Talukdar, S. Butler, S. Sampson, J. Ribeiro, S. Dell, S. Mackenzie, S. Hegarty, S. Albaba, S. McKee, S. Palmer-Smith, S. Heggarty, S. MacParland, S. Greville-Heygate, S. Daniels, S. Prapa, S. Abbs, S. Tennant, S. Hardy, S. MacMahon, S. McVeigh, T. Foo, T. Bedenham, T. Cranston, T. McDevitt, T. Clowes, V. Tripathi, V. McConnell, V. Woodwaer, N. Wallis, Y. Kemp, Z. Mullan, G. Pierson, L. Rainey, L. Joyce, C. Timbs, A. Reuther, A.-M. Frugtniet, B. DeSouza, B. Husher, C. Lawn, C. Corbett, C. Nocera-Jijon, D. Reay, D. Cross, E. Ryan, F. Lindsay, H. Oliver, J. Dring, J. Spiers, J. Harper, J. Ciucias, K. Connolly, L. Tsang, M. Brown, R. Shepherd, S. Begum, S. Daniels, S. Tadiso, T. Linton-Willoughby, T. Heppell, H. Sahan, K. Worrillow, L. Allen, Z. Watt, C. Hegarty, M. Mitchell, R. Coles, R. Nickless, G. Cojocaru, E. Doal, I. Sava, F. McCarthy, C. Jeeneea, R. Goudie, D. McConachie, M. Botosneanu, S. Kavanaugh, G. Russell, K. Sherlaw, C. Tsoulaki, O. Forde, C. Petley, E. Jones, A.-B. Oprych, K. Pryde, S. Hyder, Z. Elkhateeb, N. Braham, R. Hanington, L. Huntley, C. Irving, R. Sadan, A. Ramos, M. Elliot, C. Wren, D. Lobo, D. McLean, J. May, D. Kearney, L. Campbell, T. Asakura, K. Alwadi, L. O’Shea, R. Gabriel, J. Chiecchio, L. Bowman, P. Sutton, L.A. Walsh, C. Cloke, V. Ucanok, D. Davies, J. Pleasance, B. Maguire, E. Whaite, A. Best, S. Westbury, S. Logan, A. Navarajasegaran, D. Bench, A. Wightman, P. Cartwright, A. Higgs, E. J.Bott Whitehouse, H. Stevens, J. Martin, D. Dunlop, J. Thomas, S. Sau, C. Farndon, S. Coleman, N. Angelini, P. Duff, M. Massey, H. Rowlands, C. Garcia-Petit, C. Gillespie, K. Alder, A. Middleton, E. Cassidy, C. Orfali, N. Webb, A. Luharia, A. Walker, N. Charlton, J. Andreou, A. Peddie, J. Khan, M. Wilkinson, L. Bezuidenhout, H. Edis, M. Callard, A. Ostrowski, P. Moverley, P. Bean, K. Dunne, A. Moleirinho, A. Waller, S. Cox, K. Greensmith, L. Brittle, A. Gossan, N. Freestone, L. Shak, C. Langford, T. Clinch, Y. Livesey, H. Borland, S. Joshi, A. Wall, K. Whitworth, A. Wilsdon, A. Edgerley, K. Pugh, S. Chrysochoidi, N. Mutch, S. McMullan, C. Johnston, Y. Muraru, M. May, A. Begum, R. Smith, C. Patel, R. Bhatnagar, I. Taylor, A. Brown, D. Willan, J. Taylor, S. Jones, K. Cox, K. Ramsden, C. Taiwo, O. Jaudzemaite, J. Sharmin, R. Young, L. O’Dubhshlaine, C. McSorley, L. Rodriguez, I. Abreu Lillis, S. Alexopoulos, P. Mortensson, E. Kingham, L. Moore, R. Kosicka-Slawinska, M. Aslam, S. Wells, R. Carter, A. Warren, H. Rolf, E. Reed, H. Pearce, L. Lock, D. Ali, F. Kolozi, A. White, N. Wood, D. Hayden, C.
Source :
Genetics in Medicine; February 2025, Vol. 27 Issue: 2
Publication Year :
2025
Abstract
Current practice is to report and manage likely pathogenic/pathogenic variants in a given cancer susceptibility gene as though having equivalent penetrance, despite increasing evidence of intervariant variability in risk associations. Using existing variant interpretation approaches, largely based on full-penetrance models, variants in which reduced penetrance is suspected may be classified inconsistently and/or as variants of uncertain significance. We aimed to develop a national consensus approach for such variants within the Cancer Variant Interpretation Group UK (CanVIG-UK) multidisciplinary network.
Details
Language :
English
ISSN :
10983600 and 15300366
Volume :
27
Issue :
2
Database :
Supplemental Index
Journal :
Genetics in Medicine
Publication Type :
Periodical
Accession number :
ejs67801041
Full Text :
https://doi.org/10.1016/j.gim.2024.101305