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SMARCA4 c.1285G>A ;(p.A429T)
Variant ID: 19-11101865-G-A
NM_003072.3(
SMARCA4
):c.1285G>A;(p.A429T)
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:
Analysis of gene expression signatures identifies prognostic and functionally distinct ovarian clear cell carcinoma subtypes.
Ebiomedicine
Tan, Tuan Zea TZ; Ye, Jieru J; Yee, Chung Vin CV; Lim, Diana D; Ngoi, Natalie Yan Li NYL; Tan, David Shao Peng DSP; Huang, Ruby Yun-Ju RY
Publication Date: 2019-12
Variant appearance in text: SMARCA4: 1285G>A; A429T
PubMed Link:
31761620
Variant Present in the following documents:
mmc1.xlsx, sheet 7
View BVdb publication page
Mutation profiles of synchronous colorectal cancers from a patient with Lynch syndrome suggest distinct oncogenic pathways.
Journal Of Gastrointestinal Oncology
Wheeler, Scott R SR; Shi, Chanjuan C; Holt, Jonathan A JA; Vnencak-Jones, Cindy L CL
Publication Date: 2016-06
Variant appearance in text: SMARCA4: 1285G>A; A429T
PubMed Link:
27284491
Variant Present in the following documents:
Main text
View BVdb publication page