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PTEN c.409_411delinsTTT ;(p.A137F)
Variant ID: 10-89692925-GCA-TTT
NM_000314.4(
PTEN
):c.409_411delinsTTT;(p.A137F)
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 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: rs878853938
PubMed Link:
36561320
Variant Present in the following documents:
Table2.xlsx, sheet 6
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: A137F
PubMed Link:
31819097
Variant Present in the following documents:
Main text
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
41598_2019_Article_54976.pdf
View BVdb publication page