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CETP c.1363G>T ;(p.V455L)
Variant ID: 16-57017279-G-T
NM_000078.2(
CETP
):c.1363G>T;(p.V455L)
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:
c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.
Plos One
Ganesan, Mala M; Nizamuddin, Sheikh S; Katkam, Shiva Krishna SK; Kumaraswami, Konda K; Hosad, Uday Kumar UK; Lobo, Limmy Loret LL; Kutala, Vijay Kumar VK; Thangaraj, Kumarasamy K
Publication Date: 2016
Variant appearance in text: rs2228667
PubMed Link:
27768712
Variant Present in the following documents:
Main text
pone.0164151.pdf
View BVdb publication page
Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.
Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015
Variant appearance in text: rs2228667
PubMed Link:
26659599
Variant Present in the following documents:
pone.0144692.s002.xlsx, sheet 1
View BVdb publication page
Direct molecular haplotyping of long-range genomic DNA with M1-PCR.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Ding, Chunming C; Cantor, Charles R CR
Publication Date: 2003-06-24
Variant appearance in text: rs2228667
PubMed Link:
12802015
Variant Present in the following documents:
Main text
View BVdb publication page