CALR c.733_735del ;(p.P245del)

Variant ID: 19-13051385-CCCT-C

NM_004343.3(CALR):c.733_735del;(p.P245del)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia.

Scientific Reports
Kim, Borahm B; Yun, Woobin W; Lee, Seung-Tae ST; Choi, Jong Rok JR; Yoo, Keon Hee KH; Koo, Hong Hoe HH; Jung, Chul Won CW; Kim, Sun Hee SH
Publication Date: 2020-08-31

Variant appearance in text: CALR: 733_735delCCT; Pro245del
PubMed Link: 32868804
Variant Present in the following documents:
  • 41598_2020_71386_MOESM1_ESM.pdf
View BVdb publication page