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BRAF c.2063C>A ;(p.A688D)
Variant ID: 7-140439676-G-T
NM_004333.4(
BRAF
):c.2063C>A;(p.A688D)
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:
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: 2063C>A
PubMed Link:
28492226
Variant Present in the following documents:
ncomms15086-s3.xlsx, sheet 1
View BVdb publication page
Targeted exome sequencing reveals distinct pathogenic variants in Iranians with colorectal cancer.
Oncotarget
Ashktorab, Hassan H; Mokarram, Pooneh P; Azimi, Hamed H; Olumi, Hasti H; Varma, Sudhir S; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-01-31
Variant appearance in text: BRAF: A688D
PubMed Link:
28002797
Variant Present in the following documents:
oncotarget-08-7852-s002.xlsx, sheet 15
View BVdb publication page