12100C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001241


SNP (HGVS):

c.12100 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

12100

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Ala3945Ala

Gene

ORF1ab

Amino Acid Change:

Ala - A - alanine

Ala - A - alanine

Position in the gene

3945

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%
  • GH ( GISAID_clade ) Prevalence: 3.23%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • AY.23 ( pangolin_lineage ) Prevalence: 1.50%
  • AY.23.1 ( pangolin_lineage ) Prevalence: 0.13%
  • B.1.429 ( pangolin_lineage ) Prevalence: 0.13%

Frequency of this variation:

This variation was identified in 0.38 % of the analyzed genomes.