20178C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID002532


SNP (HGVS):

c.20178 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

20178

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Val6638Val

Gene

ORF1ab

Amino Acid Change:

Val - V - valine

Val - V - valine

Position in the gene

6638

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:

  • GRY ( GISAID_clade ) Prevalence: 5.17%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • N.10 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.24 ( pangolin_lineage ) Prevalence: 0.87%
  • C.37 ( pangolin_lineage ) Prevalence: 1.03%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • AY.4 ( pangolin_lineage ) Prevalence: 4.83%

Frequency of this variation:

This variation was identified in 0.47 % of the analyzed genomes.