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Submitted SNP(ss) Details: ss5236854562           
Submitter
HandleCPQ_GEN_INCA
Submitter SNP IDrs5751738
RefSNP(rs#)clustering in process
Submitted Batch IDHuman_Comprehensive_Cancer_Panel_blood
Submitted DateJan 27, 2021
Publication Cited[1] Analysis of retinoblastoma with a panel of 160 genes- 90 novel, somatic, pathogenic mutations
First entry to dbSNPJan 27 2021 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSUB8494678
Ascertainment Samplesize46
PopulationPanelRB
Allele
Observed AlleleG/C
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
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|ss5236854562|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic
 CTGTGTGTTA CGTGGGAACA GTCCC
 S
 TTTCCTGCCA GCTGCCTGTC AGGCA

  Submitted Frequency for ss5236854562 back to top
There is no frequency submission for ss5236854562.


  dbSNP summary of Genotypes for ss5236854562 back to top
No sufficient data to compute Hardy-weinberg probability for ss5236854562.


  Submitted individual genotype for ss5236854562 back to top
There is no individual genotype data for ss5236854562.

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