13329C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001106


SNP (HGVS):

c.13329 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

13329

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Thr4355Ile

Gene

ORF1ab

Amino Acid Change:

Thr - T - threonine

Ile - I - isoleucine

Position in the gene

4355

Position in the gene

Synonymous / Non-Synonymous:

Missense

Structural / Non-Structural Protein:

Non-Structural

Predicted effect:

MODERATE
Lineages and frequencies

variation observed in these lineages:

  • O ( GISAID_clade ) Prevalence: 1.90%
  • GRY ( GISAID_clade ) Prevalence: 5.17%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • P.1.10.1 ( pangolin_lineage ) Prevalence: 0.07%
  • AY.4 ( pangolin_lineage ) Prevalence: 4.83%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • AY.24 ( pangolin_lineage ) Prevalence: 0.87%
  • P.1 ( pangolin_lineage ) Prevalence: 3.53%
  • P.1.10 ( pangolin_lineage ) Prevalence: 0.03%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • B.6.2 ( pangolin_lineage ) Prevalence: 0.07%

Frequency of this variation:

This variation was identified in 0.12 % of the analyzed genomes.