28606C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001348


SNP (HGVS):

c.28606 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

28606

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

N : p.Tyr111Tyr

Gene

N

Amino Acid Change:

Tyr - Y - tyrosine

Tyr - Y - tyrosine

Position in the gene

111

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%
  • GH ( GISAID_clade ) Prevalence: 3.23%
  • AY.25 ( pangolin_lineage ) Prevalence: 2.50%
  • B.1.497 ( pangolin_lineage ) Prevalence: 0.03%

Frequency of this variation:

This variation was identified in 0.09 % of the analyzed genomes.