5884C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001865


SNP (HGVS):

c.5884 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

5884

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Tyr1873Tyr

Gene

ORF1ab

Amino Acid Change:

Tyr - Y - tyrosine

Tyr - Y - tyrosine

Position in the gene

1873

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:

  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GRY ( GISAID_clade ) Prevalence: 5.17%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • AY.3 ( pangolin_lineage ) Prevalence: 1.30%
  • B.1.1.389 ( pangolin_lineage ) Prevalence: 0.03%
  • P.1 ( pangolin_lineage ) Prevalence: 3.53%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • B.1.1.216 ( pangolin_lineage ) Prevalence: 0.10%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • AZ.5 ( pangolin_lineage ) Prevalence: 0.30%

Frequency of this variation:

This variation was identified in 0.17 % of the analyzed genomes.