CREBBP c.1011dup ;(p.Q338Tfs*12)

Variant ID: 16-3843591-G-GT

NM_004380.2(CREBBP):c.1011dup;(p.Q338Tfs*12)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Benign and malignant tumors in Rubinstein-Taybi syndrome.

American Journal Of Medical Genetics. Part A
Boot, Max V MV; van Belzen, Martine J MJ; Overbeek, Lucy I LI; Hijmering, Nathalie N; Mendeville, Matias M; Waisfisz, Quinten Q; Wesseling, Pieter P; Hennekam, Raoul C RC; de Jong, Daphne D
Publication Date: 2018-03

Variant appearance in text: CREBBP: 1011dupA
PubMed Link: 29359884
Variant Present in the following documents:
  • Main text
  • AJMG-176-597.pdf
View BVdb publication page



Whole exome sequencing for a patient with Rubinstein-Taybi syndrome reveals de novo variants besides an overt CREBBP mutation.

International Journal Of Molecular Sciences
Yoo, Hee Jeong HJ; Kim, Kyung K; Kim, In Hyang IH; Rho, Seong-Hwan SH; Park, Jong-Eun JE; Lee, Ki Young KY; Kim, Soon Ae SA; Choi, Byung Yoon BY; Kim, Namshin N
Publication Date: 2015-03-11

Variant appearance in text: CREBBP: 1011dupA; Gln338fs
PubMed Link: 25768348
Variant Present in the following documents:
  • ijms-16-05697-s001.pdf
View BVdb publication page