10755C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID003398


SNP (HGVS):

c.10755 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

10755

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Ala3497Val

Gene

ORF1ab

Amino Acid Change:

Ala - A - alanine

Val - V - valine

Position in the gene

3497

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%
  • AY.43 ( pangolin_lineage ) Prevalence: 2.60%
  • AY.25 ( pangolin_lineage ) Prevalence: 2.50%

Frequency of this variation:

This variation was identified in 0.08 % of the analyzed genomes.