1191C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001567


SNP (HGVS):

c.1191 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

1191

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Pro309Leu

Gene

ORF1ab

Amino Acid Change:

Pro - P - proline

Leu - L - leucine

Position in the gene

309

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:

  • S ( GISAID_clade ) Prevalence: 1.93%
  • GH ( GISAID_clade ) Prevalence: 3.23%
  • G ( GISAID_clade ) Prevalence: 6.87%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • B.1.311 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.35 ( pangolin_lineage ) Prevalence: 0.13%
  • AY.16 ( pangolin_lineage ) Prevalence: 0.27%
  • AY.5 ( pangolin_lineage ) Prevalence: 0.87%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • AY.13 ( pangolin_lineage ) Prevalence: 0.10%
  • AY.37 ( pangolin_lineage ) Prevalence: 0.70%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • AY.30 ( pangolin_lineage ) Prevalence: 0.47%
  • A.25 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.15 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.14 ( pangolin_lineage ) Prevalence: 0.17%
  • AY.11 ( pangolin_lineage ) Prevalence: 0.13%

Frequency of this variation:

This variation was identified in 0.31 % of the analyzed genomes.