10632C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001633


SNP (HGVS):

c.10632 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

10632

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Ala3456Val

Gene

ORF1ab

Amino Acid Change:

Ala - A - alanine

Val - V - valine

Position in the gene

3456

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:

  • GR ( GISAID_clade ) Prevalence: 18.10%
  • GH ( GISAID_clade ) Prevalence: 3.23%
  • P.1 ( pangolin_lineage ) Prevalence: 3.53%
  • B.1.351.2 ( pangolin_lineage ) Prevalence: 0.07%

Frequency of this variation:

This variation was identified in 0.02 % of the analyzed genomes.