18555C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID00851


SNP (HGVS):

c.18555 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

18555

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Asp6097Asp

Gene

ORF1ab

Amino Acid Change:

Asp - D - aspartic_acid

Asp - D - aspartic_acid

Position in the gene

6097

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:

  • G ( GISAID_clade ) Prevalence: 6.87%
  • S ( GISAID_clade ) Prevalence: 1.93%
  • GH ( GISAID_clade ) Prevalence: 3.23%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GRY ( GISAID_clade ) Prevalence: 5.17%
  • B.1.3 ( pangolin_lineage ) Prevalence: 0.03%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • AY.43 ( pangolin_lineage ) Prevalence: 2.60%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • AY.39.1 ( pangolin_lineage ) Prevalence: 3.03%
  • A.2.5 ( pangolin_lineage ) Prevalence: 0.57%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%

Frequency of this variation:

This variation was identified in 3.44 % of the analyzed genomes.