TP53 c.543del ;(p.C182Afs*65)

Variant ID: 17-7578387-AG-A

NM_000546.5(TP53):c.543del;(p.C182Afs*65)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Hereditary cancer syndrome-associated pathogenic variants are common in patients with hematologic malignancies subsequent to primary solid cancer.

Journal Of Cancer
Oh, Joowon J; Kim, Yu Ri YR; Kim, Yoonjung Y; Kim, Boyeon B; Park, Kyung Sun KS; Nam, Seong-Hyeuk SH; Lee, Kyung-A KA
Publication Date: 2021

Variant appearance in text: TP53: 543del
PubMed Link: 34093829
Variant Present in the following documents:
  • jcav12p4288s2.xlsx, sheet 3
View BVdb publication page