BRAF c.1695-940C>A

Variant ID: 7-140454973-G-T

NM_004333.4(BRAF):c.1695-940C>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Combined Mutational and Clonality Analyses Support the Existence of Intra-Tumor Heterogeneity in Papillary Thyroid Cancer.

Journal Of Clinical Medicine
Muzza, Marina M; Pogliaghi, Gabriele G; Persani, Luca L; Fugazzola, Laura L; Colombo, Carla C
Publication Date: 2021-06-16

Variant appearance in text: rs7801086
PubMed Link: 34208446
Variant Present in the following documents:
  • Main text
  • jcm-10-02645.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs7801086
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Polyclonality of BRAF mutations in acquired melanocytic nevi.

Journal Of The National Cancer Institute
Lin, Jingrong J; Takata, Minoru M; Murata, Hiroshi H; Goto, Yasufumi Y; Kido, Kenji K; Ferrone, Soldano S; Saida, Toshiaki T
Publication Date: 2009-10-21

Variant appearance in text: rs7801086
PubMed Link: 19752400
Variant Present in the following documents:
  • Main text
View BVdb publication page