ABCC9 p.Met1198Ile

ClinVar: c.3594G>A , p.Met1198Ile ? , Uncertain significance
Predicted by SNAP2: A: N (66%), C: N (78%), D: D (53%), E: N (53%), F: N (72%), G: N (53%), H: N (78%), I: N (82%), K: N (57%), L: N (87%), N: N (78%), P: D (59%), Q: N (72%), R: N (61%), S: N (82%), T: N (87%), V: N (78%), W: N (53%), Y: N (78%),
Predicted by PROVEAN: A: D, C: D, D: D, E: D, F: D, G: D, H: D, I: N, K: D, L: N, N: D, P: D, Q: D, R: D, S: D, T: D, V: N, W: D, Y: D,

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[hide] Waldmuller S, Schroeder C, Sturm M, Scheffold T, Imbrich K, Junker S, Frische C, Hofbeck M, Bauer P, Bonin M, Gawaz M, Gramlich M
Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
Mol Cell Probes. 2015 Oct;29(5):308-14. doi: 10.1016/j.mcp.2015.05.004. Epub 2015 May 12., [PMID:25979592]

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