29477G>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID002548


SNP (HGVS):

c.29477 G > T

Nucleotide in reference genome:

G - (Guanine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

29477

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

N : p.Asp402Tyr

Gene

N

Amino Acid Change:

Asp - D - aspartic_acid

Tyr - Y - tyrosine

Position in the gene

402

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%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • G ( GISAID_clade ) Prevalence: 6.87%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • B.1.380 ( pangolin_lineage ) Prevalence: 0.17%
  • P.1 ( pangolin_lineage ) Prevalence: 3.53%

Frequency of this variation:

This variation was identified in 0.07 % of the analyzed genomes.