Overview
Nucleotide ID | | c.1151_1154delinsCGTGTC |
| | |
Protein ID | | p.D384Afs*47 |
| | |
Mutation | | Deletion+Insertion |
| | |
Type | | Type 2-like |
| | |
Class | | Class B |
| | |
Category | | #NA |
COSMIC | | #NA |
| | |
Pathologie | | Essential thrombocythaemia |
Structure
# PSIPRED HFORMAT (PSIPRED V4.0)
Conf: 935766237899999999999999999999999999999999999999999999994399
Pred: CHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCC
AA: AAEKQMKDKQDEEQRLKEEEEDKKRKEEEEAEACRRMMRTKMRMRRMRRTRRKMRRKMSP
10 20 30 40 50 60
Conf: 999954999998535139
Pred: CCCCCCHHHHHHHHHHCC
AA: ARPRTSCREACLQGWTEA
70
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 |