ABCA4 p.Ser795Arg

Predicted by SNAP2: A: N (72%), C: N (57%), D: N (61%), E: N (66%), F: D (59%), G: N (72%), H: N (66%), I: N (57%), K: N (72%), L: D (53%), M: D (53%), N: N (82%), P: N (57%), Q: N (66%), R: N (66%), T: N (82%), V: N (57%), W: D (80%), Y: D (53%),
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,

[switch to compact view]
Comments [show]
Publications
[hide] Downs K, Zacks DN, Caruso R, Karoukis AJ, Branham K, Yashar BM, Haimann MH, Trzupek K, Meltzer M, Blain D, Richards JE, Weleber RG, Heckenlively JR, Sieving PA, Ayyagari R
Molecular testing for hereditary retinal disease as part of clinical care.
Arch Ophthalmol. 2007 Feb;125(2):252-8., [PMID:17296903]

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

[hide] Alapati A, Goetz K, Suk J, Navani M, Al-Tarouti A, Jayasundera T, Tumminia SJ, Lee P, Ayyagari R
Molecular diagnostic testing by eyeGENE: analysis of patients with hereditary retinal dystrophy phenotypes involving central vision loss.
Invest Ophthalmol Vis Sci. 2014 Jul 31;55(9):5510-21. doi: 10.1167/iovs.14-14359., [PMID:25082885]

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