BRAF c.1694A>G ;(p.D565G)

Variant ID: 7-140476712-T-C

NM_004333.4(BRAF):c.1694A>G;(p.D565G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Circulating tumour DNA sequence analysis as an alternative to multiple myeloma bone marrow aspirates.

Nature Communications
Kis, Olena O; Kaedbey, Rayan R; Chow, Signy S; Danesh, Arnavaz A; Dowar, Mark M; Li, Tiantian T; Li, Zhihua Z; Liu, Jessica J; Mansour, Mark M; Masih-Khan, Esther E; Zhang, Tong T; Bratman, Scott V SV; Oza, Amit M AM; Kamel-Reid, Suzanne S; Trudel, Suzanne S; Pugh, Trevor J TJ
Publication Date: 2017-05-11

Variant appearance in text: BRAF: 1694A>G
PubMed Link: 28492226
Variant Present in the following documents:
  • ncomms15086-s3.xlsx, sheet 1
View BVdb publication page



Diagnosis of Noonan syndrome and related disorders using target next generation sequencing.

Bmc Medical Genetics
Lepri, Francesca Romana FR; Scavelli, Rossana R; Digilio, Maria Cristina MC; Gnazzo, Maria M; Grotta, Simona S; Dentici, Maria Lisa ML; Pisaneschi, Elisa E; Sirleto, Pietro P; Capolino, Rossella R; Baban, Anwar A; Russo, Serena S; Franchin, Tiziana T; Angioni, Adriano A; Dallapiccola, Bruno B
Publication Date: 2014-01-23

Variant appearance in text: BRAF: 1694A>G; D565G
PubMed Link: 24451042
Variant Present in the following documents:
  • Main text
  • 1471-2350-15-14.pdf
View BVdb publication page