HPV Mutation Detail Information

> A6964C Search Result


Mutation Information
Mutation Site A6964C
Mutation Type Nucleotide level
Gene/Protein/Region Type L1
Nucleotide_Mutation K442N
Genotype/Subtype HPV16
Viral Reference U89348
Country India
Literature Information
PubMed PMID 18199779
Disease Cervical carcinoma
Published Year 2008
Journal Journal of clinical microbiology
Title Human papillomavirus type 16 variant analysis of E6, E7, and L1 genes and long control region in biopsy samples from cervical cancer patients in north India.
Author Pande S,Jain N,Prusty BK,Bhambhani S,Gupta S,Sharma R,Batra S,Das BC
Evidence Of four variants found independently (Fig. ​(Fig.2),2), two were silent mutations, A6667C and A6691G, coding for serine at codons 343 and 351, whereas A6803T and A6964C led to the missense mutations threonine→serine (T389S) and lysine→asparagine (K442N). The most frequently detected L1 variation, A6695C (Fig. ​(Fig.1c),1c), was found in six (54.5%) cases.

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Description
Mutation Information Note
  • Gene/Protein/Region Type: Virus Gene (e.g. LMP-1) or Virus Protein (e.g. Rep 68) or Virus Region (e.g. S, X)
Literature Information Note
  • Evidence: sentence contains this mutation information in the citation