Overview



Nucleotide ID c.1122_1123delinsTTGT
Protein ID p.K374Nfs*57
Mutation Deletion+Insertion
Type Type other
Class Class C (C1)
Category #NA
COSMIC COSV57120413
Pathologie Essential thrombocythaemia


Structure

# PSIPRED HFORMAT (PSIPRED V4.0)


Conf: 935764027789999999985756999999999999999999999999999999994399


Pred: CHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCC


  AA: AAEKQMKDKQDEEQRLKEEEEDNCNAKRRRRQRTRRMMRTKMRMRRMRRTRRKMRRKMSP


              10        20        30        40        50        60


Conf: 999832999998202129


Pred: CCCCCCHHHHHHHHHHCC


  AA: ARPRTSCREACLQGWTEA


              70

References

PMIDCitation
25746303Li N, Yao QM, Gale RP, et al. Frequency and allele burden of CALR mutations in Chinese with essential thrombocythemia and primary myelofibrosis without JAK2(V617F) or MPL mutations. Leuk Res. 2015.39(5):510-514. doi:10.1016/j.leukres.2015.02.006