27869T>C IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID004815


SNP (HGVS):

c.27869 T > C

Nucleotide in reference genome:

T - (Thymine)

Nucleotide in target genome:

C - (Cytosine)

Position in the genome:

27869

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF7b : p.Asn38Asn

Gene

ORF7b

Amino Acid Change:

Asn - N - asparagine

Asn - N - asparagine

Position in the gene

38

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:

  • GRY ( GISAID_clade ) Prevalence: 5.17%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%

Frequency of this variation:

This variation was identified in 0.03 % of the analyzed genomes.