24138C>A IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001894


SNP (HGVS):

c.24138 C > A

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

A - (Adenine)

Position in the genome:

24138

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

S : p.Thr859Asn

Gene

S

Amino Acid Change:

Thr - T - threonine

Asn - N - asparagine

Position in the gene

859

Position in the gene

Synonymous / Non-Synonymous:

Missense

Structural / Non-Structural Protein:

Structural

Predicted effect:

MODERATE
Lineages and frequencies

variation observed in these lineages:

  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GH ( GISAID_clade ) Prevalence: 3.23%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • C.1.2 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.46.6 ( pangolin_lineage ) Prevalence: 0.20%
  • B.1.626 ( pangolin_lineage ) Prevalence: 0.07%
  • C.37 ( pangolin_lineage ) Prevalence: 1.03%
  • C.37.1 ( pangolin_lineage ) Prevalence: 0.03%

Frequency of this variation:

This variation was identified in 0.13 % of the analyzed genomes.