BRAF c.1799_1816del ;(p.V600_S605del)

Variant ID: 7-140453118-CCACTCCATCGAGATTTCA-C

NM_004333.4(BRAF):c.1799_1816del;(p.V600_S605del)

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:

Clinical-Pathological and Molecular Evaluation of 451 NIFTP Patients from a Single Referral Center.

Cancers
Vignali, Paola P; Proietti, Agnese A; Macerola, Elisabetta E; Poma, Anello Marcello AM; Torregrossa, Liborio L; Ugolini, Clara C; Basolo, Alessio A; Matrone, Antonio A; Rago, Teresa T; Santini, Ferruccio F; Elisei, Rossella R; Materazzi, Gabriele G; Basolo, Fulvio F
Publication Date: 2022-01-14

Variant appearance in text: BRAF: V600_S605del
PubMed Link: 35053581
Variant Present in the following documents:
  • Main text
  • cancers-14-00420.pdf
View BVdb publication page


Clinical-Pathological and Molecular Evaluation of 451 NIFTP Patients from a Single Referral Center.

Cancers
Vignali, Paola P; Proietti, Agnese A; Macerola, Elisabetta E; Poma, Anello Marcello AM; Torregrossa, Liborio L; Ugolini, Clara C; Basolo, Alessio A; Matrone, Antonio A; Rago, Teresa T; Santini, Ferruccio F; Elisei, Rossella R; Materazzi, Gabriele G; Basolo, Fulvio F
Publication Date: 2022-01-14

Variant appearance in text: BRAF: V600_S605del
PubMed Link: 35053581
Variant Present in the following documents:
  • Main text
  • cancers-14-00420.pdf
View BVdb publication page