23929C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID002008


SNP (HGVS):

c.23929 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

23929

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

S : p.Tyr789Tyr

Gene

S

Amino Acid Change:

Tyr - Y - tyrosine

Tyr - Y - tyrosine

Position in the gene

789

Position in the gene

Synonymous / Non-Synonymous:

Synonymous

Structural / Non-Structural Protein:

Structural

Predicted effect:

LOW
Lineages and frequencies

variation observed in these lineages:

  • G ( GISAID_clade ) Prevalence: 6.87%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • O ( GISAID_clade ) Prevalence: 1.90%
  • L ( GISAID_clade ) Prevalence: 0.67%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • B.6 ( pangolin_lineage ) Prevalence: 0.40%
  • B.1 ( pangolin_lineage ) Prevalence: 2.40%
  • B.6.8 ( pangolin_lineage ) Prevalence: 0.10%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • B.6.1 ( pangolin_lineage ) Prevalence: 0.03%
  • B.6.2 ( pangolin_lineage ) Prevalence: 0.07%
  • B.6.6 ( pangolin_lineage ) Prevalence: 0.03%
  • P.1 ( pangolin_lineage ) Prevalence: 3.53%

Frequency of this variation:

This variation was identified in 0.56 % of the analyzed genomes.