21800G>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID003974


SNP (HGVS):

c.21800 G > T

Nucleotide in reference genome:

G - (Guanine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

21800

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

S : p.Asp80Tyr

Gene

S

Amino Acid Change:

Asp - D - aspartic_acid

Tyr - Y - tyrosine

Position in the gene

80

Position in the gene

Synonymous / Non-Synonymous:

Missense

Structural / Non-Structural Protein:

Structural

Predicted effect:

MODERATE
Lineages and frequencies

variation observed in these lineages:

  • S ( GISAID_clade ) Prevalence: 1.93%
  • G ( GISAID_clade ) Prevalence: 6.87%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • O ( GISAID_clade ) Prevalence: 1.90%
  • B.1.380 ( pangolin_lineage ) Prevalence: 0.17%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • C.36 ( pangolin_lineage ) Prevalence: 0.13%
  • AY.33 ( pangolin_lineage ) Prevalence: 1.03%
  • AZ.5 ( pangolin_lineage ) Prevalence: 0.30%
  • B.1.1.404 ( pangolin_lineage ) Prevalence: 0.07%
  • A.2.5 ( pangolin_lineage ) Prevalence: 0.57%
  • B.1.524 ( pangolin_lineage ) Prevalence: 0.10%

Frequency of this variation:

This variation was identified in 0.38 % of the analyzed genomes.