Overview
Nucleotide ID | | c.1135_1147del |
| | |
Protein ID | | p.E379Rfs*47 |
| | |
Mutation | | Deletion |
| | |
Type | | Type other |
| | |
Class | | Class C (C1) |
| | |
Category | | #NA |
COSMIC | | #NA |
| | |
Pathologie | | Myelofibrosis / Essential thrombocythaemia |
Structure
# PSIPRED HFORMAT (PSIPRED V4.0)
Conf: 936776238889999999999999999999999999999999999999999449999994
Pred: CHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCC
AA: AAEKQMKDKQDEEQRLKEEEEDKKRKERTRRMMRTKMRMRRMRRTRRKMRRKMSPARPRT
10 20 30 40 50 60
Conf: 3999998202139
Pred: CHHHHHHHHHHCC
AA: SCREACLQGWTEA
70
References
PMID | Citation |
---|
29424450 | Lasho TL, Finke CM, Tischer A, Pardanani A, Tefferi A. Mayo CALR mutation type classification guide using alpha helix propensity. Am J Hematol. 2018.93(5):E128-E129. doi:10.1002/ajh.25065 |