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PTEN c.421C>G ;(p.H141D)
Variant ID: 10-89692937-C-G
NM_000314.4(
PTEN
):c.421C>G;(p.H141D)
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:
Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.
Frontiers In Genetics
G, Vigneshwaran V; Hasan, Qurratulain Annie QA; Kumar, Rahul R; Eranki, Avinash A
Publication Date: 2022
Variant appearance in text: PTEN: H141D
PubMed Link:
36561320
Variant Present in the following documents:
Table3.xlsx, sheet 1
Table2.xlsx, sheet 6
View BVdb publication page
Robotic complete mesocolic excision using indocyanine fluorescence imaging in colorectal cancer: A case study and technical approach.
International Journal Of Surgery Case Reports
Young, R R; Rajkomar, A K S AKS; Smart, P P; Warrier, S K SK
Publication Date: 2020
Variant appearance in text: PTEN: H141D
PubMed Link:
32248014
Variant Present in the following documents:
Main text
main.pdf
View BVdb publication page
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: PTEN: H141D
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page