26882C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID002587


SNP (HGVS):

c.26882 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

26882

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

M : p.Leu120Leu

Gene

M

Amino Acid Change:

Leu - L - leucine

Leu - L - leucine

Position in the gene

120

Position in the gene

Synonymous / Non-Synonymous:

Synonymous

Structural / Non-Structural Protein:

Structural

Predicted effect:

LOW
Lineages and frequencies

variation observed in these lineages:

  • GK ( GISAID_clade ) Prevalence: 58.57%
  • GRY ( GISAID_clade ) Prevalence: 5.17%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • AY.34 ( pangolin_lineage ) Prevalence: 0.73%

Frequency of this variation:

This variation was identified in 0.1 % of the analyzed genomes.