ABCC7 p.Ala566Pro

ClinVar: c.1696G>A , p.Ala566Thr ? , not provided
CF databases: c.1697C>A , p.Ala566Asp (CFTR1) D , He originated from the Esfahan province in the centre of Iran.
c.1696G>A , p.Ala566Thr (CFTR1) ? , This mutation was detected by SSCP/HA analysis and confirmed by bi-directional sequencing. The patient's other mutation is deltaF508. Both the patient's parents are Swedish in origin. The patient was referred to Manchester for analysis from the Adult CF Centre at Papworth Hospital, Cambridge by Dr Bilton
Predicted by SNAP2: C: N (72%), D: D (75%), E: D (75%), F: D (66%), G: N (53%), H: D (66%), I: D (59%), K: D (71%), L: D (63%), M: D (53%), N: N (78%), P: D (63%), Q: D (63%), R: D (66%), S: N (66%), T: N (53%), V: N (53%), W: D (75%), Y: D (66%),
Predicted by PROVEAN: C: D, D: D, E: D, F: D, G: D, H: D, I: D, K: D, L: D, M: D, N: D, P: D, Q: D, R: D, S: N, T: D, V: D, W: D, Y: D,

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[hide] Mendoza JL, Schmidt A, Li Q, Nuvaga E, Barrett T, Bridges RJ, Feranchak AP, Brautigam CA, Thomas PJ
Requirements for efficient correction of DeltaF508 CFTR revealed by analyses of evolved sequences.
Cell. 2012 Jan 20;148(1-2):164-74. doi: 10.1016/j.cell.2011.11.023., [PMID:22265409]

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