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Submitted SNP(ss) Details: ss2625678804           
Submitter
HandleSYSTEMSBIOZJU
Submitter SNP IDSYSTEMSBIOZJU_SNV1810964
RefSNP(rs#)rs5859643
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 AlleleA/-
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss2625678804|allelePos=26|len=51|taxid=9606|alleles='A/-'|mol=Genomic
 TTAATATTTG TCTCAGTTGT CTGCC
 N
 AAAAAAAAAA AAAATGTAAA TTCAC

  Submitted Frequency for ss2625678804 back to top
There is no frequency submission for ss2625678804.


  dbSNP summary of Genotypes for ss2625678804 back to top
No sufficient data to compute Hardy-weinberg probability for ss2625678804.


  Submitted individual genotype for ss2625678804 back to top
There is no individual genotype data for ss2625678804.

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