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F2 c.1196_1197delinsAA ;(p.R399Q)
Variant ID: 11-46749611-GC-AA
NM_000506.3(
F2
):c.1196_1197delinsAA;(p.R399Q)
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:
Association of DNA Repair Genes XRCC1 and APE-1 with the Risk of Cervical Cancer in North Indian population.
Asian Pacific Journal Of Cancer Prevention : Apjcp
Charles, Mark Rector MR; Raza, Syed Tasleem ST; Sharma, Rolee R; Pratap, Pushpendra P; Eba, Ale A; Singh, Manvendra M
Publication Date: 2020-07-01
Variant appearance in text: F2: Arg399Gln
PubMed Link:
32711433
Variant Present in the following documents:
Main text
APJCP-21-2061.pdf
View BVdb publication page
Polymorphisms of DNA repair genes OGG1 and XPD and the risk of age-related cataract in Egyptians.
Molecular Vision
Gharib, Amal F AF; Dabour, Sherif A SA; Etewa, Rasha L RL; Fouad, Rania A RA
Publication Date: 2014
Variant appearance in text: F2: Arg399Gln
PubMed Link:
24868140
Variant Present in the following documents:
mv-v20-661.pdf
View BVdb publication page
Association of betel nut with carcinogenesis: revisit with a clinical perspective.
Plos One
Sharan, Rajeshwar N RN; Mehrotra, Ravi R; Choudhury, Yashmin Y; Asotra, Kamlesh K
Publication Date: 2012
Variant appearance in text: F2: Arg399Gln
PubMed Link:
22912735
Variant Present in the following documents:
Main text
pone.0042759.pdf
View BVdb publication page