24914G>C IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID0047


SNP (HGVS):

c.24914 G > C

Nucleotide in reference genome:

G - (Guanine)

Nucleotide in target genome:

C - (Cytosine)

Position in the genome:

24914

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

S : p.Asp1118His

Gene

S

Amino Acid Change:

Asp - D - aspartic_acid

His - H - histidine

Position in the gene

1118

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%
  • G ( GISAID_clade ) Prevalence: 6.87%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • O ( GISAID_clade ) Prevalence: 1.90%
  • B.1.1.7 ( pangolin_lineage ) Prevalence: 8.40%
  • Q.1 ( pangolin_lineage ) Prevalence: 0.10%
  • B.1.1 ( pangolin_lineage ) Prevalence: 2.77%
  • Q.8 ( pangolin_lineage ) Prevalence: 0.07%
  • B.1.620 ( pangolin_lineage ) Prevalence: 0.27%
  • Q.3 ( pangolin_lineage ) Prevalence: 0.03%

Frequency of this variation:

This variation was identified in 20.36 % of the analyzed genomes.