Overview
Nucleotide ID | | c.1115_1139del |
| | |
Protein ID | | p.E372Gfs*50 |
| | |
Mutation | | Deletion |
| | |
Type | | Type other |
| | |
Class | | Class C (C1) |
| | |
Category | | #NA |
COSMIC | | #NA |
| | |
Pathologie | | Essential thrombocythaemia |
Structure
# PSIPRED HFORMAT (PSIPRED V4.0)
Conf: 935766127779999999999999999999999999999999999993499999954999
Pred: CHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCHHH
AA: AAEKQMKDKQDEEQRLKEEEGRQRTRRMMRTKMRMRRMRRTRRKMRRKMSPARPRTSCRE
10 20 30 40 50 60
Conf: 998535139
Pred: HHHHHHHCC
AA: ACLQGWTEA
References
PMID | Citation |
---|
35016075 | Fabris S, Cattaneo D, Salerio S, et al. Impact on thrombotic risk of canonical and atypical CALR mutations in essential thrombocythemia. A single-center cohort study. Thromb Res. 2022.210:67-69. doi:10.1016/j.thromres.2021.12.021 |