Overview



Nucleotide ID c.1103_1148del
Protein ID p.K368Rfs*47
Mutation Deletion
Type Type 1-like
Class Class A
Category #NA
COSMIC COSV57116851
Pathologie Myelofibrosis / Essential thrombocythaemia


Structure

# PSIPRED HFORMAT (PSIPRED V4.0)


Conf: 935764027549999999999999999999999999999943999998329999982131


Pred: CHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHCCCCCCCCCHHHHHHHHHH


  AA: AAEKQMKDKQDEEQRLRTRRMMRTKMRMRRMRRTRRKMRRKMSPARPRTSCREACLQGWT


              10        20        30        40        50        60


Conf: 29


Pred: CC


  AA: EA

References

PMIDCitation
25729726Park SH, Kim SY, Lee SM, et al. Incidence, clinical features, and prognostic impact of CALR exon 9 mutations in essential thrombocythemia and primary myelofibrosis: an experience of a single tertiary hospital in Korea. Ann Lab Med. 2015.35(2):233-237. doi:10.3343/alm.2015.35.2.233