CALR c.1145C>T ;(p.A382V)

Variant ID: 19-13054618-C-T

NM_004343.3(CALR):c.1145C>T;(p.A382V)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Targeted sequencing of candidate gene regions for myelofibrosis in dogs.

Journal Of Veterinary Internal Medicine
Campbell, Amelia G AG; Seelig, Davis M DM; Beckman, Joan D JD; Minor, Katie M KM; Heinrich, Daniel A DA; Friedenberg, Steven G SG; Modiano, Jaime F JF; Furrow, Eva E
Publication Date: 2022-07

Variant appearance in text: CALR: A382V
PubMed Link: 35815881
Variant Present in the following documents:
  • JVIM-36-1237-s003.xlsx, sheet 1
View BVdb publication page



Full spectrum of clonal haematopoiesis-driver mutations in chronic heart failure and their associations with mortality.

Esc Heart Failure
Kiefer, Katharina C KC; Cremer, Sebastian S; Pardali, Evangelia E; Assmus, Birgit B; Abou-El-Ardat, Khalil K; Kirschbaum, Klara K; Dorsheimer, Lena L; Rasper, Tina T; Berkowitsch, Alexander A; Serve, Hubert H; Dimmeler, Stefanie S; Zeiher, Andreas M AM; Rieger, Michael A MA
Publication Date: 2021-06

Variant appearance in text: CALR: 1145C>T; A382V
PubMed Link: 33779075
Variant Present in the following documents:
  • EHF2-8-1873-s002.xlsx, sheet 1
View BVdb publication page