ABCC7 p.Tyr517Ile

CF databases: c.1549T>C , p.Tyr517His (CFTR1) ? , 1540del10 mutation was found in the other allele, which was inherited from her healthy Japanese mother.
c.1550A>G , p.Tyr517Cys (CFTR1) ? , The mutation was detected by SSCP analysis and identified by direct DNA sequencing and confirmed by restriction site generated PCR: a modified primer creates a RsaI site, destroyed by the mutation.
Predicted by SNAP2: A: D (80%), C: D (66%), D: D (91%), E: D (91%), F: D (63%), G: D (85%), H: D (80%), I: D (66%), K: D (91%), L: D (53%), M: D (80%), N: D (91%), P: D (95%), Q: D (85%), R: D (91%), S: D (85%), T: D (85%), V: D (66%), W: D (75%),
Predicted by PROVEAN: A: D, 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: D, T: D, V: D, W: 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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