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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