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PC c.1801C>G ;(p.L601V)
Variant ID: 11-66619934-G-C
NM_001040716.1(
PC
):c.1801C>G;(p.L601V)
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:
A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.
Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12
Variant appearance in text: PC: L601V
PubMed Link:
34253785
Variant Present in the following documents:
41598_2021_93715_MOESM3_ESM.xlsx, sheet 5
View BVdb publication page
The importance of CDC27 in cancer: molecular pathology and clinical aspects.
Cancer Cell International
Kazemi-Sefat, Golnaz Ensieh GE; Keramatipour, Mohammad M; Talebi, Saeed S; Kavousi, Kaveh K; Sajed, Roya R; Kazemi-Sefat, Nazanin Atieh NA; Mousavizadeh, Kazem K
Publication Date: 2021-03-09
Variant appearance in text: PC: 1801C>G
PubMed Link:
33750395
Variant Present in the following documents:
12935_2021_Article_1860.pdf
View BVdb publication page