1267C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001568


SNP (HGVS):

c.1267 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

1267

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Gly334Gly

Gene

ORF1ab

Amino Acid Change:

Gly - G - glycine

Gly - G - glycine

Position in the gene

334

Position in the gene

Synonymous / Non-Synonymous:

Synonymous

Structural / Non-Structural Protein:

Non-Structural

Predicted effect:

LOW
Lineages and frequencies

variation observed in these lineages:

  • G ( GISAID_clade ) Prevalence: 6.87%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • AY.30 ( pangolin_lineage ) Prevalence: 0.47%
  • AY.15 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.13 ( pangolin_lineage ) Prevalence: 0.10%
  • AY.37 ( pangolin_lineage ) Prevalence: 0.70%
  • AY.33 ( pangolin_lineage ) Prevalence: 1.03%
  • AY.35 ( pangolin_lineage ) Prevalence: 0.13%
  • AY.16 ( pangolin_lineage ) Prevalence: 0.27%
  • AY.14 ( pangolin_lineage ) Prevalence: 0.17%
  • AY.11 ( pangolin_lineage ) Prevalence: 0.13%
  • AY.36 ( pangolin_lineage ) Prevalence: 0.43%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%

Frequency of this variation:

This variation was identified in 0.04 % of the analyzed genomes.