12439C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID003727


SNP (HGVS):

c.12439 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

12439

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Pro4058Pro

Gene

ORF1ab

Amino Acid Change:

Pro - P - proline

Pro - P - proline

Position in the gene

4058

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:

  • GK ( GISAID_clade ) Prevalence: 58.57%
  • G ( GISAID_clade ) Prevalence: 6.87%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • B.1 ( pangolin_lineage ) Prevalence: 2.40%
  • B.1.380 ( pangolin_lineage ) Prevalence: 0.17%
  • AY.39 ( pangolin_lineage ) Prevalence: 2.27%
  • AY.47 ( pangolin_lineage ) Prevalence: 0.27%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • AY.25 ( pangolin_lineage ) Prevalence: 2.50%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • P.1 ( pangolin_lineage ) Prevalence: 3.53%

Frequency of this variation:

This variation was identified in 0.19 % of the analyzed genomes.