17126T>C IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID004939


SNP (HGVS):

c.17126 T > C

Nucleotide in reference genome:

T - (Thymine)

Nucleotide in target genome:

C - (Cytosine)

Position in the genome:

17126

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Leu5621Pro

Gene

ORF1ab

Amino Acid Change:

Leu - L - leucine

Pro - P - proline

Position in the gene

5621

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:

  • GK ( GISAID_clade ) Prevalence: 58.57%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%

Frequency of this variation:

This variation was identified in 0.06 % of the analyzed genomes.