ABCC7 p.Ser466Thr

ClinVar: c.1397C>T , p.Ser466Leu ? , not provided
c.1397C>G , p.Ser466* D , Pathogenic
c.1397C>A , p.Ser466* D , Pathogenic
CF databases: c.1397C>A or c.1397C>G , p.Ser466* D , CF-causing
c.1397C>T , p.Ser466Leu (CFTR1) D , The above mutation was detected by DGGE and identified by direct sequencing in an infertile man with isolated CBAVD.
Predicted by SNAP2: A: D (80%), C: D (85%), D: D (91%), E: D (91%), F: D (91%), G: D (85%), H: D (91%), I: D (91%), K: D (91%), L: D (91%), M: D (91%), N: D (85%), P: D (91%), Q: D (91%), R: D (95%), T: D (75%), V: D (91%), W: D (95%), Y: D (95%),
Predicted by PROVEAN: A: N, 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, T: N, 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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