17690C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID0066


SNP (HGVS):

c.17690 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

17690

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Ser5809Leu

Gene

ORF1ab

Amino Acid Change:

Ser - S - serine

Leu - L - leucine

Position in the gene

5809

Position in the gene

Synonymous / Non-Synonymous:

Missense

Structural / Non-Structural Protein:

Non-Structural

Predicted effect:

MODERATE
Lineages and frequencies

variation observed in these lineages:

  • G ( GISAID_clade ) Prevalence: 6.87%
  • B.1.147 ( pangolin_lineage ) Prevalence: 0.07%

Frequency of this variation:

This variation was identified in 0.09 % of the analyzed genomes.