4276C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001166


SNP (HGVS):

c.4276 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

4276

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Tyr1337Tyr

Gene

ORF1ab

Amino Acid Change:

Tyr - Y - tyrosine

Tyr - Y - tyrosine

Position in the gene

1337

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:

  • G ( GISAID_clade ) Prevalence: 6.87%
  • GK ( GISAID_clade ) Prevalence: 58.57%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • AY.4 ( pangolin_lineage ) Prevalence: 4.83%
  • B.1.23 ( pangolin_lineage ) Prevalence: 0.07%
  • AY.21 ( pangolin_lineage ) Prevalence: 0.03%
  • AY.43 ( pangolin_lineage ) Prevalence: 2.60%
  • B.1.617.2 ( pangolin_lineage ) Prevalence: 27.27%
  • C.37 ( pangolin_lineage ) Prevalence: 1.03%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%

Frequency of this variation:

This variation was identified in 0.15 % of the analyzed genomes.