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PTEN c.256G>C ;(p.A86P)
Variant ID: 10-89692772-G-C
NM_000314.4(
PTEN
):c.256G>C;(p.A86P)
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:
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma.
Cell Death & Disease
Choi, Seung Won SW; Lee, Yeri Y; Shin, Kayoung K; Koo, Harim H; Kim, Donggeon D; Sa, Jason K JK; Cho, Hee Jin HJ; Shin, Hye-Mi HM; Lee, Se Jeong SJ; Kim, Hyunho H; Chung, Seok S; Shin, Jihye J; Lee, Cheolju C; Nam, Do-Hyun DH
Publication Date: 2021-04-07
Variant appearance in text: PTEN: 256G>C; A86P
PubMed Link:
33828082
Variant Present in the following documents:
41419_2021_3657_MOESM15_ESM.pdf
View BVdb publication page
Structural and functional impact of cancer-related missense somatic mutations.
Journal Of Molecular Biology
Shi, Zhen Z; Moult, John J
Publication Date: 2011-10-21
Variant appearance in text: PTEN: A86P
PubMed Link:
21763698
Variant Present in the following documents:
Main text
View BVdb publication page
Predicting the functional impact of protein mutations: application to cancer genomics.
Nucleic Acids Research
Reva, Boris B; Antipin, Yevgeniy Y; Sander, Chris C
Publication Date: 2011-09-01
Variant appearance in text: PTEN: A86P
PubMed Link:
21727090
Variant Present in the following documents:
supp_gkr407_Supplement2_Table_SM1_COSMIC_mutations.xls, sheet 1
View BVdb publication page