SARS_CoV_2 mutation literature information.


  SARS-CoV-2 genomic variations associated with mortality rate of COVID-19.
 PMID: 32699345       2020       Journal of human genetics
Result: Comparing the mutations among the three clusters, the average frequency of an L variant of an ORF1ab P4715L in the countries classified as the cluster 1 was 14.7%, which is significantly lower than 81.3% and 73.2%, respectively, in the countries classified as the clusters 2 and 3 (P = 1.3 x 10-6 and P = 2.5 x 10-5, respectively; Supplementary.
Result: We finally searched peptide epitopes with a high binding affinity to HLA molecules, which we previously reported, involving the two SARS-CoV-2 mutations, ORF1ab P4715L and S D614G, to investigate the association with host immune responses.
Result: We found that several epitopes, which include the position of ORF1ab P4715L<


  SARS-CoV-2 Genomes From Oklahoma, United States.
 PMID: 33613621       2020       Frontiers in genetics
Abstract: Previously reported mutations including D614G in S gene, P4715L in ORF1ab, S194L, R203K, and G204R in N gene were identified in the genomes sequenced in this study.
Introduction: P4715L in ORF1ab is believed to play a major role in interaction with other proteins that regulate RNA dependent RNA polymerase.
Introduction: SNPs in the genome that result in commonly reported non-synonymous mutations such as P4715L in ORF1ab, D614G in S g


  Variant analysis of SARS-CoV-2 genomes.
 PMID: 32742035       2020       Bulletin of the World Health Organization
Abstract: The most common variants were the synonymous 3037C > T (6334 samples), P4715L in the open reading frame 1ab (6319 samples) and D614G in the spike protein (6294 samples).
Result: Most samples in the D614G clade also display the non-coding variant 241C > T, the synonymous variant 3037C > T and ORF1ab 
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.


  SARS-CoV-2 genomic surveillance in Taiwan revealed novel ORF8-deletion mutant and clade possibly associated with infections in Middle East.
 PMID: 32543353       2020       Emerging microbes & infections
Result: In addition to the signature mutation S-D614G annotated by GISAID in clade III, all the Taiwanese genomes shared two ORF1ab mutations C2772T and C14144T (P4715L) (Figure 3E).


  Evolutionary and structural analyses of SARS-CoV-2 D614G spike protein mutation now documented worldwide.
 PMID: 32820179       2020       Scientific reports
Introduction: For example, most strains of the D614G clade also harbor a mutation (P4715L) in orf1ab and a subclade processes three nucleotide changes in the nucleoprotein (N) gene (GGG to AAC; G204R), which plays diverse roles in virion assembly as well as genome transcription and translation.


  A SARS-CoV-2 vaccine candidate would likely match all currently circulating variants.
 PMID: 32868447       2020       Proc Natl Acad Sci U S A
Result: Across the genome, there were, on average, 4.05 nucleotide mutations per individual genome when compared to the consensus, with only P4715L and D614G found in >50% of sequences.
Result: Since the beginning of the pandemic, two mutations across the genome have become consensus: P4715L in ORF1ab (nucleotide 14,143, C to T) and D614G in S (nucleotide 23,403, A to G).
Figure: (B) Phylogenetic tree reconstructed from all of the ORFs showing the linkage between D614G in S and P4715L in ORF1ab.


  SARS-CoV-2 genomic and quasispecies analyses in cancer patients reveal relaxed intrahost virus evolution.
 PMID: 32869023       2020       bioRxiv
Result: Four genetically linked mutations previously described as the globally dominant haplotype in April 2020 were found in the majority of our consensus sequences: C241T (100%; 5'UTR region), C3037T (98.6%; silent mutation), C14408T (100%; resulting in P4715L/P323L amino acid change in ORF1ab) and A23403G (100%; resulting in D614G amino acid change in S).


  BioAider: An efficient tool for viral genome analysis and its application in tracing SARS-CoV-2 transmission.
 PMID: 32904401       2020       Sustainable cities and society
Table: P4715L


  A persistently replicating SARS-CoV-2 variant derived from an asymptomatic individual.
 PMID: 32967693       2020       Journal of translational medicine
Result: Alignment analyses showed that, with respect to the Wuhan-Hu-1 Reference Genome NC_045512.2, SARS-CoV-UNIBS-2 AP66 consensus sequence displayed 6 nucleotide substitutions (C241T; C3037T; C14408T; T21784G; C21846T; A23403G) leading to 4 non-synonymous changes (ORF1ab polypeptide: P4715L; S protein: N74K, T95I, D614G).
Result: Less pathogenic GZ69 consensus sequence differed from Wuhan-Hu-1 isolate in 11 nucleotide positions (C241T; C2939T; C3037T


  SARS-CoV-2 gene content and COVID-19 mutation impact by comparing 44 Sarbecovirus genomes.
 PMID: 33024961       2020       Research square
Result: Spike D614G was nearly always co-inherited with Pol P4715L (also radical and altering a perfectly-conserved residue in a highly-conserved context, but potentially-deleterious given Pol's slow evolution and less-likely-to-be-adaptive function), nsp3 nucleotide change C3037T (repeatedly-observed synonymous change, outside synonymously-constrained elements, likely-neutral), and nucleotide change C241T (perfectly-conserved, non-coding, in a loop of six unpaired bases in the conserved 5'UTR SL5B secondary structure 25 nucleotides upstream of ORF1ab).



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