NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss2137334800           
Submitter
HandleSYSTEMSBIOZJU
Submitter SNP IDSYSTEMSBIOZJU_SNV45134
RefSNP(rs#)rs1293703493
Submitted Batch IDWhole_Genome_Sequencing
Submitted DateJan 06, 2017
Publication Cited[1] Whole genome sequencing of matched tumor, adjacent non-tumor tissue and corresponding normal blood samples of hepatocellular carcinoma patients revealed a TP53 (R249S) mutation associated with poor prognosis
First entry to dbSNPJan 6 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodRESEQ
Ascertainment Samplesize2
Populationhepatocellular carcinoma patients
Allele
Observed Allele-/TAGCGCCCCTTGC
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss2137334800|allelePos=26|len=51|taxid=9606|alleles='-/TAGCGCCCCTTGC'|mol=Genomic
 AGTGTCTCCC ACAGACCCAC ATGAG
 N
 TACTCTCCAG GCGCTCTTCA GGCAG

  Submitted Frequency for ss2137334800 back to top
There is no frequency submission for ss2137334800.


  dbSNP summary of Genotypes for ss2137334800 back to top
No sufficient data to compute Hardy-weinberg probability for ss2137334800.


  Submitted individual genotype for ss2137334800 back to top
There is no individual genotype data for ss2137334800.