SARS_CoV_2 mutation literature information.


  Omicron: A Heavily Mutated SARS-CoV-2 Variant Exhibits Stronger Binding to ACE2 and Potently Escapes Approved COVID-19 Therapeutic Antibodies.
 PMID: 35140714       2021       Frontiers in immunology
Introduction: The non-structural proteins encoded by the ORF1ab contain mutations in the nsp3 (K38R, V1069I, Delta1265, L1266I, A1892T), nsp4 (T492I), nsp5 (P132H), nsp6 (Delta105-107, A189V), nsp12 (P323L), and nsp14 (I42V).


  Importation, circulation, and emergence of variants of SARS-CoV-2 in the South Indian state of Karnataka.
 PMID: 35243004       2021       Wellcome open research
Discussion: The lineage is characterized by the following amino acid replacements- nsp12-P323L(95.38%), S-D614G (93.85%), S-N440K (56.92%), ORF 3a-Q57H (90.77%), ORF 3a-E261*(81.54%), nsp3-T183I (81.54%), nsp16-L126F(80%), N-S2P (72.31%), ORF 8-S97I (72.31%) (extended data, Supplementary Table 7 ).


  Mutations in SARS-CoV-2 viral RNA identified in Eastern India: Possible implications for the ongoing outbreak in India and impact on viral structure and host susceptibility.
 PMID: 32515358       2020       Journal of biosciences
Result: These consisted of the 14408 C/T mutation resulting in a change of P323L in the RdRp and
Table: P323L
Discussion: In particular, the P323L was present in all A2a sequences in our samples.


  An updated analysis of variations in SARS-CoV-2 genome.
 PMID: 32595352       2020       Turkish journal of biology
Result: C14408T variation observed to be responsible from P323L exchange causing a missense mutation.
Table: P323L


  Identification of the nucleotide substitutions in 62 SARS-CoV-2 sequences from Turkey.
 PMID: 32595354       2020       Turkish journal of biology
Table: P323L
Discussion: C14408T mutation within the RNA-dependent RNA polymerase encoding region of ORF1b, which is a missense mutation that leads to an amino acid change from proline to leucine at position 323 (P323L) in RNA polymerase protein, was amongst the most commonly seenmutations [61% (38/62)] in isolates from Turkey.


  Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus.
 PMID: 32697968       2020       Cell
5Result: At that time, the G614 form was rare globally but gaining prominence in Europe, and GISAID was also tracking the clade carrying the D614G substitution, designating it the ""G clade."" The
Figure: Of note, the TTCG form did not expand, and it lacked the RdRp P323L change, raising the possibility that the P323L change may contribute to a selective advantage of the haplotype.
Figure: One is in the RdRp protein (nucleotide C14408T resulting in a P323L amino acid change), one in Spike (nucleotide A23403G resulting in the D614G amino acid change) and one is silent (C3037T).


  Variant analysis of SARS-CoV-2 genomes.
 PMID: 32742035       2020       Bulletin of the World Health Organization
Result: The most common variants were the synonymous variant 3037C > T (6334 samples), ORF1ab P4715L (RdRp P323L; 6319 samples) and SD614G (6294 samples).
Result: We also detected mutations in the nonstructural protein RNA-dependent RNA polymerase (RdRp), such as P323L (6319 samples).
Discussion: Almost all strains with D614G mutation also have a mutation in the protein responsible for replication (ORF1ab P4715L; RdRp P323L), which might affect replication speed of the virus.


  RdRp mutations are associated with SARS-CoV-2 genome evolution.
 PMID: 32742818       2020       PeerJ
Introduction: The proline to leucine substitution (P323L) caused by the 14408C>T mutation has been suggested to rigidify the RdRp protein structure, which may exert its effects through altered interaction with other components of the replication/transcription machinery or with the RNA template, thereby resulting in an altered mutation rate.
Result: Although preliminary studies suggest that 14408C>T (P323L in RdRp) could lower replication fidelity, it is less clear how the synonymous 15324C>T mutation could lead to lower mutation rates.


  Characterizing SARS-CoV-2 mutations in the United States.
 PMID: 32818213       2020       Research square
Introduction: Based on genotyping results, top eight missense mutations (i.e., 14408C>T-(P323L), 23403A>G-(D614G), 25563G>T-(Q57H), 1059C>T-(T85I), 28144T>C-(L84S), 17858A>G-(Y541C), 17747C>T-(P504L), and 27964C>T-(S24L)) are identified, in addition to three synonymous mutations (i.e., 3037C>T-(F106F), 8782C>T-(


  Molecular Epidemiology Analysis of SARS-CoV-2 Strains Circulating in Romania during the First Months of the Pandemic.
 PMID: 32823907       2020       Life (Basel, Switzerland)
Result: These mutations, C3037T, C14408T (P323L in Nsp12) and A23403G (D614G in S), were present in all Romanian sequences.
Result: When looking into the GISAID database mutational statistics, which uses hCoV-19/Wuhan/WIV04/2019 EPI_ISL_402124 as a reference strain (COVsurver tool), both P323L and D614G mutations are present in a high percentage (61.7%/61.8%, n = 33480 and n = 33537).



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