17747C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001990


SNP (HGVS):

c.17747 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

17747

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Pro5828Leu

Gene

ORF1ab

Amino Acid Change:

Pro - P - proline

Leu - L - leucine

Position in the gene

5828

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:

  • S ( GISAID_clade ) Prevalence: 1.93%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • A.1 ( pangolin_lineage ) Prevalence: 0.03%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%

Frequency of this variation:

This variation was identified in 1.11 % of the analyzed genomes.