27765C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID001827


SNP (HGVS):

c.27765 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

27765

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF7b : p.Leu4Phe

Gene

ORF7b

Amino Acid Change:

Leu - L - leucine

Phe - F - phenylalanine

Position in the gene

4

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%
  • B.1.1.274 ( pangolin_lineage ) Prevalence: 0.03%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • C.37 ( pangolin_lineage ) Prevalence: 1.03%

Frequency of this variation:

This variation was identified in 0.05 % of the analyzed genomes.