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PARP4 c.3838G>T ;(p.G1280C)
Variant ID: 13-25009441-C-A
NM_006437.3(
PARP4
):c.3838G>T;(p.G1280C)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.
Nature Communications
Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B
Publication Date: 2020-04-09
Variant appearance in text: PARP4: G1280C
PubMed Link:
32273506
Variant Present in the following documents:
41467_2020_15456_MOESM6_ESM.xlsx, sheet 1
41467_2020_15456_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page
Molecular Classification and Pharmacogenetics of Primary Plasma Cell Leukemia: An Initial Approach toward Precision Medicine.
International Journal Of Molecular Sciences
Simeon, Vittorio V; Todoerti, Katia K; La Rocca, Francesco F; Caivano, Antonella A; Trino, Stefania S; Lionetti, Marta M; Agnelli, Luca L; De Luca, Luciana L; Laurenzana, Ilaria I; Neri, Antonino A; Musto, Pellegrino P
Publication Date: 2015-07-30
Variant appearance in text: PARP4: Gly1280Cys; rs13428
PubMed Link:
26263974
Variant Present in the following documents:
Main text
View BVdb publication page