19018C>T IDbSV - International Database of SARS-CoV-2 Variants
SNP

SNP: ID003874


SNP (HGVS):

c.19018 C > T

Nucleotide in reference genome:

C - (Cytosine)

Nucleotide in target genome:

T - (Thymine)

Position in the genome:

19018

SARS-CoV-2 genes

Annotation


Amino Acid Mutation (HGVS):

ORF1ab : p.Pro6252Ser

Gene

ORF1ab

Amino Acid Change:

Pro - P - proline

Ser - S - serine

Position in the gene

6252

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:

  • GH ( GISAID_clade ) Prevalence: 3.23%
  • GR ( GISAID_clade ) Prevalence: 18.10%
  • B.1.1.312 ( pangolin_lineage ) Prevalence: 0.10%
  • B.1.429 ( pangolin_lineage ) Prevalence: 0.13%

Frequency of this variation:

This variation was identified in 0.04 % of the analyzed genomes.