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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs715313          
refSNP ID: rs715313
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:86/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
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 ss15994756 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs715313 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
ss27475TSC-CSHL|TSC0005239byFreqfwd/TA/Gagccacacctctgatccaatttctttaccctaactcaacagaatctattctattctctcc09/06/0004/07/0486Genomic95 %
ss3583293SC_JCM|AC009522.8_19392fwd/TA/Gagccacacctctgatccaatttctttaccctaactcaacagaatctattctattctctcc09/24/0110/10/03100Genomicunknown
ss4108309SC_JCM|AC009522.10_20732fwd/TA/Gagccacacctctgatccaatttctttaccctaactcaacagaatctattctattctctcc10/15/0110/10/03101Genomicunknown
ss12218761WI_SSAHASNP|chr12.NT_019546.15_13735486rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct07/04/0310/10/03116Genomicunknown
ss14530460WUGSC_SSAHASNP|chr12.NT_019546.15_13735486rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct11/05/0310/25/06119Genomicunknown
ss15994756SC_SNP|NT_019546.15_13735486byFreqrev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct11/18/0310/26/06120Genomicunknown
ss16598787CSHL-HAPMAP|CSHL-HuAA-200402.chr12.NT_019546.15_13735486rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct02/17/0403/04/04120Genomicunknown
ss20938497SSAHASNP|WGSA-200403-chr12.chr12.NT_019546.15_13735486rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct03/19/0403/19/04121Genomicunknown
ss24707400PERLEGEN|afd2072558byFreqrev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct08/10/0409/13/04123Genomicunknown
ss38886939ABI|hCV2406463rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct07/16/0507/16/05126Genomicunknown
ss65990608AFFY|SNP_A-1676249rev/BC/Tgaatagaatagattctgttgagttagggtaaagaaattggatcagaggtg10/26/0610/26/06127Genomicunknown
ss82668375HGSV|Cor18555_SNV_20070510.chr12_88755763rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct11/27/0712/03/07130Genomicunknown
ss89307546BCMHGSC_JDW|JWB-0592784rev/BC/Tggagagaatagaatagattctgttgagttagggtaaagaaattggatcagaggtgtggct02/26/0802/28/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs715313|allelePos=712|totalLen=1607|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 AGCCAAAAGT CCCAGAGACA CATACAAACC TCCAGAGAAC TTAGACATTT GAAATCCATG
 ACACTCAGAC AAGGTCTTAT TACATCAGTT GGGTTTTGCT GTGTAAGAAA CTACACCCAA
 AACTGGGTGT CTTAAAATAA TAGTCATTGT TCTGTGAATC AATAATTTGG GCTGGACTTT
 GCTGGGAAGT TCTTCTGCTA GAATTGGCAA GGCTCACCCA TGCAGCTGCA GTCAGTGAGT
 AGATCAGCTA GGGAGTGATT CAACATCTCA CTCAATGTTT GGTGGCTGGT ACTGTCAGTT
 GTTGTTGGCT GCCAGCAGAG TGACAGAGGT GACTGGCCAC AGGTCTCCAG CAAATTGCTC
 CAGGTTTATA TTTACCTGGT TGCAGTCACA AGGCTCCCAA AAGCAGCAAG AGTGGGCAAG
 CCCCAATACA CAATCATATT TCAAGCTTCT GTTTGTATCA CATTTGCTAA TGGCCCATTG
 ATCACAATAA AGCCACATCA CCAAGCCCAG CTCAAAGGGT GAGGAAATAA ACTCCACCTC
 TTGATGGGAG TAGCTGCAAA GAAATATTGC AAAGGGACAG GCAAACAGGT AGAAGATTTT
 ATAACCATGT CTGCAGTCTG CCACATTTTT CTCTCTTCTT CCTTCATTAA CTTCACTTTT
 TCACTACCCA TTCATGCCTC AAGCCACACC TCTGATCCAA TTTCTTTACC C
 R
 TAACTCAACA GAATCTATTC TATTCTCTCC CAAATTACTA ATGACCTCTT TGTTTCTGGC
 TAAGTCCAGG GGACCTTTTT CTCTCATTGT CTCATTTGGA GTCTCAGTGT CACTTGACGC
 AATCTTCTCC ATTGACTTTG ATAGTACTAC TCTTTTCCTT CTTTTCCTCT TAGCTGTTTC
 TTCACAGTCT CCTGCATAGA AAAAGTGGGT AGCAGGGCAC CTAGCACAAA ATATGCATTT
 AAAATTGATT TGTTGAATAA ATGATTAAGT GAATAAATTA ATGAACAAAT AAAATGGGAT
 TATGTTCTAC CCACTGATTA AATGTTGGAG TTTGTAAAGC TTCAGCTACT ACCTATGTGC
 TAACGACTTC CAATTACAAG TCTCCAGCCC AGGTCTCTTT TCTGCACTCA GGCATATGTA
 TGCAGCCTCT GAATAGACTC TTCTCACTGA CACTTCAAAC TCAACCTATC TGAATCTGAT
 CTCATTAACC TCACTTCCAG ATCTGCTTTT CTTTCAAATT CTTTCACGAT CTACACAGTC
 ACCAAAGCCA AACATTTGAG TGTCATTCTA GGCTCCTTCC TATGTGGCAC CAAGTCTTAC
 TGCTTTATCA TTATGTTTTG TTTCATTTTG AGACAGGGTC TCACACTGTC ATCTAGATTG
 GAGTACAGTG GTATGTACTG CAGCCTCCAC CTTGTGGGCT CAAGCAATCC TCCTACCTCA
 GGCTCCTGAG TAGCTGAGAC TACAGGCATG AGCCACCACA ACGAGTTAAT TTTTTAATTT
 TTATTTTGGA AGGACGAGAT CTCACTATTT TGCTCAGGCT GGTCTCAAAC TCCTTCTGCC
 TTGGCCTCCC AACGTGCTAG GCTTTAATTT TTTTTTTTTA ATTTGCTGCC TTCTC

  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:  rs715313 maps exactly once on NCBI human chromosome 12
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
12NW_001838061.21912069887319170plusAalt_assembly_8HuRefHuRefview711
12NT_019546.151373548688777426minusCref_assemblyreferencereferenceview711
12NW_925395.13754879889924969minusTalt_assembly_1CeleraCeleraview711

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_019546 AC009522.3 AC084200
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss15994756HapMap-CEUEuropean 120IG 0.633 0.350 0.017 0.317 0.808 0.192
HapMap-HCBAsian 90IG 0.800 0.200 0.479 0.900 0.100
HapMap-JPTAsian 88IG 0.727 0.273 0.294 0.864 0.136
HapMap-YRISub-Saharan African 118IG 0.915 0.085 0.752 0.958 0.042
ss24707400AFD_EUR_PANELEuropean 46IG 0.609 0.391 0.251 0.804 0.196
AFD_AFR_PANELAfrican American 46IG 0.783 0.217 0.584 0.891 0.109
AFD_CHN_PANELAsian 48IG 0.750 0.250 0.527 0.875 0.125
ss27475AfAmAfrican American 12IG 0.667 0.333 0.655 0.833 0.167
CaucasianEuropean 24IG 0.750 0.167 0.083 0.200 0.833 0.167
AsianAsian 12IG 0.500 0.500 0.439 0.750 0.250
CEPHEuropean 12IG 0.667 0.167 0.167 0.200 0.750 0.250
PDpanelGlobal 48IG 0.667 0.292 0.042 1.000 0.812 0.188

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.234+/-0.250380307150

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqbySubmitterwith2hitwithHapMapFreq
Validated by: PERLEGEN
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .