26947C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID00875


SNP (HGVS):

c.26947 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

26947

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

M : p.Ala142Val

Gene

M

Amino Acid Change:

Ala - A - alanine

Val - V - valine

Position in the gene

142

Position in the gene

Synonymous / Non-Synonymous:

Missense

Structural / Non-Structural Protein:

Structural

Predicted effect:

MODERATE
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.