ABCC7 p.His609Thr

ClinVar: c.1826A>T , p.His609Leu ? , not provided
c.1826A>G , p.His609Arg ? , not provided
CF databases: c.1826A>G , p.His609Arg (CFTR1) ? , This mutation was detected by DGGE and identified by direct sequencing. H609R is not found in 100 other non-[delta]F508 CF chromosomes and 100 non CF chromosomes tested. The mutation creates an MaeII site. It was found in a CF patient originating from Columbia.
c.1826A>T , p.His609Leu (CFTR1) ? , This mutation was identified on one Italian CF chromosome
Predicted by SNAP2: A: D (66%), C: D (66%), D: D (85%), E: D (80%), F: D (75%), G: D (75%), I: D (75%), K: D (80%), L: D (75%), M: D (75%), N: D (71%), P: D (85%), Q: N (57%), R: D (75%), S: D (66%), T: D (53%), V: D (71%), W: D (85%), Y: N (72%),
Predicted by PROVEAN: A: D, C: D, D: D, E: D, F: N, G: D, I: N, K: D, L: N, M: N, N: D, P: D, Q: D, R: D, S: D, T: D, V: N, W: D, Y: N,

[switch to compact view]
Comments [show]
Publications
[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]

Abstract [show]
Comments [show]
Sentences [show]