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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs956311          
refSNP ID: rs956311
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:G/T
Ancestral Allele:G
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 ss44488530 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs956311 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
ss1401561TSC-CSHL|TSC0149774byFreqfwd/BG/Tacatacatacttcctctcagcaatagatgagacattttggactcagccacctaatgacag09/06/0004/07/0486Genomic95 %
ss6470414WI_SSAHASNP|NT_006342.13_568354rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt02/12/0310/10/03111Genomicunknown
ss10125657BCM_SSAHASNP|chr4.NT_006316.15_863739rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt06/27/0310/10/03116Genomicunknown
ss17000587CSHL-HAPMAP|CSHL-HuAA-200402.chr4.NT_006316.15_863739rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt02/17/0403/04/04120Genomicunknown
ss22088183SSAHASNP|WGSA-200403-chr4.chr4.NT_006316.15_863739rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt03/20/0403/20/04121Genomicunknown
ss44488530ABI|hCV3286758byFreqrev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt07/19/0511/03/06126Genomicunknown
ss65955615AFFY|SNP_A-1684152fwd/BG/Tcatacttcctctcagcaatagatgagacattttggactcagccacctaat10/26/0610/26/06127Genomicunknown
ss66100690AFFY|SNP_A-1975945byFreqfwd/BG/Ttctcagcaatagatgagacattttggactcag10/27/0608/14/07127Genomicunknown
ss76067132AFFY|AFFY_6_1M_SNP_A-1975945fwd/BG/Ttctcagcaatagatgagacattttggactcag08/28/0708/29/07129Genomicunknown
ss77287817HGSV|Cor12156_SNV_20070510.chr4_9864650rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt10/09/0710/12/07129Genomicunknown
ss82092604HGSV|Cor18555_SNV_20070510.chr4_9864650rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt11/27/0712/02/07130Genomicunknown
ss92467652BCMHGSC_JDW|JWB-1736230rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt02/26/0803/03/08129Genomicunknown
ss1129102041000GENOMES|CEU.trio.12.15.2008_913571_chr4_9797479rev/TA/Cctgtcattaggtggctgagtccaaaatgtctcatctattgctgagaggaagtatgtatgt12/15/0812/18/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs956311|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=130
 TCCTCATGCT AACAACAGTC TTTAAAACCT TAAGATGACT GGAAAACTTG TGAATCATTT
 GAAACCCTTT AGTGGAAGAG TGAAGAACTT GAGTTTTTAA ACCTAACAGA TGGATGATAA
 TATGGACAAT CCAAGGTCAC GGTGGTTTTA TAGTTGAGAA AACCGACACA TAATGACACC
 ATCTAGAGGC CACACAGGGC AGTTCTGGCA CAGCTGTCCT GGCTTTCCCA CACTTGCTCC
 AGCAGACACC CTGGAGCCCA GAAGCTCCCA ACATACATAC TTCCTCTCAG CAATAGATGA
 K
 GACATTTTGG ACTCAGCCAC CTAATGACAG GGTGTCACCC CCACTGCACT GCTGCTTTCC
 TATGATTGGT TTGACAGCTC ACAATGGCTA GGTTCTAAGA TTCAGGTCAA ATATGAGTCT
 GTCTGAGCAA CCTTAAACAT GGTGAGAGGT TACAGCACTA GTTCATTGTG GAGGCATTTG
 TACAACTTCC TGCATTAAGA ACAGGGGCAC AACAGAACAA CAAAAATCAA AGCAGGTAAT
 ACTGTATTAG TTCCCTGCAA GTGTTCCACA AGGCCAGAAG TACCTTCTGG TCCTCAGTAA

  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:  rs956311 maps exactly once on NCBI human chromosome 4
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
4NW_001838900.18011369521803minusCalt_assembly_8HuRefHuRefview300
4NT_006316.158637399797479minusCref_assemblyreferencereferenceview300
4NW_922073.179776610671024minusCalt_assembly_1CeleraCeleraview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_006316 AC009528.7
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceG/G
G/T
T/T
HWPG
T
ss1401561AfAmAfrican American 40IG 0.500 0.350 0.150 0.371 0.675 0.325
CaucasianEuropean 38IG 0.053 0.421 0.526 0.752 0.263 0.737
AsianAsian 40IG 0.200 0.350 0.450 0.273 0.375 0.625
CEPHEuropean 54IG 0.074 0.556 0.370 0.273 0.352 0.648
PDpanelGlobal 48IG 0.250 0.292 0.458 0.100 0.396 0.604
ss44488530HapMap-CEUEuropean 120IG 0.117 0.333 0.550 0.200 0.283 0.717
HapMap-HCBAsian 90IG 0.178 0.644 0.178 0.050 0.500 0.500
HapMap-JPTAsian 90IG 0.178 0.422 0.400 0.584 0.389 0.611
HapMap-YRISub-Saharan African 118IG 0.339 0.525 0.136 1.000 0.602 0.398
ss66100690HapMap-CEUEuropean 118GF 0.102 0.339 0.559 0.271 0.729
HapMap-HCBAsian 90GF 0.178 0.644 0.178 0.500 0.500
HapMap-JPTAsian 90GF 0.178 0.422 0.400 0.389 0.611
HapMap-YRISub-Saharan African 120GF 0.333 0.517 0.150 0.592 0.408

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.491+/-0.0663793172740ALFRED: The Allele Frequency Database

  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 .