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TG c.3905C>T ;(p.P1302L)
Variant ID: 8-133920488-C-T
NM_003235.4(
TG
):c.3905C>T;(p.P1302L)
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:
HaploCoV: unsupervised classification and rapid detection of novel emerging variants of SARS-CoV-2.
Communications Biology
Chiara, Matteo M; Horner, David S DS; Ferrandi, Erika E; Gissi, Carmela C; Pesole, Graziano G
Publication Date: 2023-04-22
Variant appearance in text: TG: 3905C>T; P1302L
PubMed Link:
37087497
Variant Present in the following documents:
42003_2023_4784_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page
Whole-Genome Sequencing of Vero E6 (VERO C1008) and Comparative Analysis of Four Vero Cell Sublines.
Frontiers In Genetics
Konishi, Kazuhiro K; Yamaji, Toshiyuki T; Sakuma, Chisato C; Kasai, Fumio F; Endo, Toshinori T; Kohara, Arihiro A; Hanada, Kentaro K; Osada, Naoki N
Publication Date: 2022
Variant appearance in text: TG: 3905C>T; Pro1302Leu
PubMed Link:
35391802
Variant Present in the following documents:
DataSheet1.xlsx, sheet 2
View BVdb publication page