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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs309136          
refSNP ID: rs309136
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:79/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/T
Ancestral Allele:A
Clinical Association:unknown
HGVS Names
Links , Linkout

SNP Details are organized in the following sections:
Submission Fasta Resource GeneView Map Diversity Validation

  Submitter records for this RefSNP Cluster back to top
The submission ss1708885 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs309136 during BLAST analysis for the current build.

NCBI
Assay ID
Handle|Submitter IDValidation
Status
ss to rs
Orientation
/Strand
Alleles5' Near Seq 30 bp3' Near Seq 30 bpEntry
Date
Update
Date
Build
Added
Molecule
Type
Freq
Warning
Ancestral
Allele
Success
Rate
ss397342KWOK|OVLP-000621-235536fwd/BA/Taccccttcaccacatcatgtgctgccagtctcacttctgctgttgccaccaaccctcgcg06/30/0010/10/0379Genomic99 %
ss750867SC_JCM|AC011999.4_78574fwd/BA/Taccccttcaccacatcatgtgctgccagtctcacttctgctgttgccaccaacccttgcg07/27/0010/10/0385Genomicunknown
ss1156506KWOK|OVLP-000804-484641fwd/BA/Taccccttcaccacatcatgtgctgccagtctcacttctgctgttgccaccaaccctcgcg09/02/0010/10/0386Genomic99 %
ss1708885KWOK|OVLP-000925-573382byFreqfwd/BA/Taccccttcaccacatcatgtgctgccagtctcacttctgctgttgccaccaaccctcgcg10/05/0008/14/0787Genomic99 %
ss44362425ABI|hCV1061811fwd/A/Taccccttcaccacatcatgtgctgccagtctcacttctgctgttgccaccaacccttgcg07/18/0507/18/05126Genomicunknown
ss66479538AFFY|SNP_A-2290327byFreqrev/TA/Tgcaacagcagaagtgagactggcagcacatga10/29/0608/14/07127Genomicunknown
ss76294069AFFY|AFFY_6_1M_SNP_A-2290327rev/A/Tgcaacagcagaagtgagactggcagcacatga08/28/0708/30/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs309136|allelePos=1118|totalLen=1318|taxid=9606|snpclass=1|alleles='A/T'|mol=Genomic|build=129
 CTTTGCATAG AGTCAACGTT GAAGGACAAG CAACTTCAAA TTTCCAAGCA ACAAAATTAT
 GTTCGGGTGG TTTTCTGAAA GCGAGATCTT AAGAACCACC TGTATCAGAA TCCCATGAAG
 AGCTTGTTTA GTGTGCAAAT TTACAGATTG TCCCCCCTCA GAAATGCTCA TTTAGgagtt
 cctgtccttt gcggggacat ggatgaagct ggaaaccatc attctcagca aactaacaca
 ggaacagaaa accaaacact gcatgttctc actcaaaagt gggagttgaa caatgagaac
 acatggacac agggagggga acgtcacaca ccagggcctg tcgggggtgg gaggtaaggg
 gagggagagg attaggacaa atacctaatg catgtggggc ttaaaaccta gatgatgggt
 tgataggtgc agcaaaccac catggacatg tatacctatg taacaaactt gcatgttcag
 tacatgtatc ccagaactta aagtaaaata TAAACCAATA ATAAAAAGGA AATGCTCATT
 CAGGAGTTTT GGGGTGGGGG TTCAGGAGGC TGCAGCCTTA ACAATTACCT CTGGTGATTT
 TGACACAGGT AGCACAGCAG CCAAACTTGG AGAGATTTGT TCACAGCACT GCATCACCAA
 CCTTACTTTC TGTTAGGCCT TTAATCACtt tttttttttt tttttttttc tgagacaggg
 tcttgctcta tcacccaggc tggagtacag tggcacgatc ttggctcact gcaatctctg
 tatcctgggt tcaagcaatc ctctctgcct tggcctcctg agtagctggg accacagaca
 tgctccatta tgcccaacta attaaaaaca ttttttttag aggcaggctg gtctcgaact
 cctgagctca agcaatctgc ctgcctcggc ctcccaaagt gctgggatta caggtgtgag
 ccactgcgcc cggccTTTTA ATCACTTTTA AACCAGCAAC CCTAATCTGC CTGTCCCTTG
 AATGGATCCG GATAAAGGTG TGGCAAACAA GCCTCCTGTC ACAGTGGGGT GTGACAGTCA
 CGGCATCACC CCTTCACCAC ATCATGTGCT GCCAGTC
 W
 TCACTTCTGC TGTTGCCACC AACCCTCGCG TTTCCCTTTG TCACTTCCCC CTTGCCACCA
 CCAACGGCCA CTGTCCCTCT GCTCCTCACC CTCCATAGCT GAGTCAGATC CAGCATTGGG
 CACTTGAGGA AGAAGCCACT GTGGAAGGCG GGATGAGGGT GTTCCCATTC TACATTCACA
 AGCCCACAGC TTGGAGAAGA

  GeneView back to top
GeneView: no link established by analysis of contig annotation
GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs309136 maps exactly once on NCBI human chromosome 2
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
2NW_001838859.212930665128758691minusTalt_assembly_8HuRefHuRefview1117
2NW_921585.14666450130476647plusAalt_assembly_1CeleraCeleraview1117
2NT_022135.1525473846136482394plusAref_assemblyreferencereferenceview1117

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
AC011999.6 AC016516 AC016516.3
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/T
HWPA
T
ss1708885HapMap-CEUEuropean 120IG 1.000 1.000
HapMap-HCBAsian 90IG 1.000 1.000
HapMap-JPTAsian 90IG 1.000 1.000
HapMap-YRISub-Saharan African 116IG 0.862 0.138 0.931 0.069
ss66479538HapMap-CEUEuropean 118GF 1.000 1.000
HapMap-HCBAsian 90GF 0.978 0.022 0.989 0.011
HapMap-JPTAsian 90GF 1.000 1.000
HapMap-YRISub-Saharan African 120GF 0.850 0.150 0.925 0.075
ss750867TSC_42_AA 84AF 1.000
TSC_42_C 84AF 1.000
TSC_42_A 84AF 1.000
Concordant GenotypeTotal SampleA/AA/T
ss170888526925413
ss6647953826814
RefSNP Genotype SummaryTotal IndividualA/AA/T
rs30913627025414
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss)GenotypePopulation
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
5159ss1708885A/ACSHL-HAPMAPHapMap-HCBNA18542CH18542r23_ch2_HCB_affymetrix:genechip500k
5159ss66479538A/TCSHL-HAPMAPHapMap-HCBNA18542CH18542chr2-HapMap-HCB
Genotype data submitted for270 samples from270 individualsIndividual with multiple genotypes submission:269

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwithHapMapFreqUNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .