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BRAF c.763C>T ;(p.L255F)
Variant ID: 7-140501309-G-A
NM_004333.4(
BRAF
):c.763C>T;(p.L255F)
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:
Deep phenotyping and whole-exome sequencing improved the diagnostic yield for nuclear pedigrees with neurodevelopmental disorders.
Molecular Genetics & Genomic Medicine
Wang, Qingqing Q; Tang, Xia X; Yang, Ke K; Huo, Xiaodong X; Zhang, Hui H; Ding, Keyue K; Liao, Shixiu S
Publication Date: 2022-05
Variant appearance in text: BRAF: 763C>T
PubMed Link:
35266334
Variant Present in the following documents:
MGG3-10-e1918.pdf
View BVdb publication page
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: 763C>T
PubMed Link:
28492226
Variant Present in the following documents:
ncomms15086-s3.xlsx, sheet 1
View BVdb publication page