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BRAF c.1799del ;(p.V600Gfs*50)
Variant ID: 7-140453136-CA-C
NM_004333.4(
BRAF
):c.1799del;(p.V600Gfs*50)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Clinical associations and genetic interactions of oncogenic BRAF alleles.
Peerj
Wagner, Sebastian A SA
Publication Date: 2022
Variant appearance in text: BRAF: V600Gfs*50
PubMed Link:
36275468
Variant Present in the following documents:
peerj-10-14126.pdf
View BVdb publication page
Clinicopathological features of rare BRAF mutations in Korean thyroid cancer patients.
Journal Of Korean Medical Science
Cho, Uiju U; Oh, Woo Jin WJ; Bae, Ja Seong JS; Lee, Sohee S; Lee, Young Sub YS; Park, Gyeong Sin GS; Lee, Youn Soo YS; Jung, Chan Kwon CK
Publication Date: 2014-08
Variant appearance in text: BRAF: 1799del
PubMed Link:
25120313
Variant Present in the following documents:
Main text
jkms-29-1054.pdf
View BVdb publication page