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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs809721          
refSNP ID: rs809721
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:C/T
Ancestral Allele:T
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 ss43571100 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs809721 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
ss1051439KWOK|OVLP-000804-267828fwd/BC/Tcctaactttggagtcttctgtcccagttccgagaaattctattttgtaatttcaccatac09/02/0010/10/0386Genomic95 %
ss1914130KWOK|OVLP-000925-521305fwd/BC/Tcctaactttggagtcttctgtcccagttccgagaaattctattttgtaatttcaccatac10/06/0010/10/0387Genomic99 %
ss1938867KWOK|OVLP-000925-512187fwd/BC/Tcctaactttggagtcttctgtcccagttccgagaaattctattttgtaatttcaccatac10/06/0010/10/0387Genomic98 %
ss2481848SC_JCM|AC012407.4_91705fwd/BC/Tcctaactttggagtcttctgtcccagttccgagaaattctattttgtaatttcaccatac11/03/0010/10/0392Genomicunknown
ss12288001WI_SSAHASNP|chr14.NT_026437.10_32652057rev/TA/Ggtatggtgaaattacaaaatagaatttctcggaactgggacagaagactccaaagttagg07/04/0310/10/03116Genomicunknown
ss21187839SSAHASNP|WGSA-200403-chr14.chr14.NT_026437.10_32652057rev/TA/Ggtatggtgaaattacaaaatagaatttctcggaactgggacagaagactccaaagttagg03/19/0403/19/04121Genomicunknown
ss43571100ABI|hCV3226991byFreqrev/TA/Ggtatggtgaaattacaaaatagaatttctcggaactgggacagaagactccaaagttagg07/18/0503/31/08126Genomicunknown
ss76816181AFFY|AFFY_6_1M_SNP_A-8677779fwd/BC/Tcttctgtcccagttccgagaaattctattttg08/28/0708/30/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs809721|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 CTACAGTGGC TTACAACTCC GTATTTATCC TAGGAACCCT AAGATTACAA ATACCTTTTA
 AAGAAAACAA CCCCAAAGTG TGACTGTTGG GCCAGCTGTG GGTCCTTGAT AAGGTTTACA
 TACATCATGC TTTAAGGTTG AAGGTTTTGA ACAAGTGCAA TTCAGGAAAC CACACGTTTC
 CTCTCAGCCA CTGTAGCTGG CCTTTACGAT GGGGTTTCCG GTTGCCTTTC CTGATTGCTT
 TGCTGGTGTC CACCCTACCC TGTTCTCAGG CCTAACTTTG GAGTCTTCTG TCCCAGTTCC
 Y
 GAGAAATTCT ATTTTGTAAT TTCACCATAC AACCAAGAAA AGTATCATTT GTTCATGCGT
 CAAATAGTTT TTGAGCTCCT ACTCTGTGCC AAGCATGGGG GTGAGGGGAT GAAGCATGTG
 GGCACTGAGG GGCATACAAC AGATAAGGAA AGGCAAACAT CATGTCGTGT GACCTCTACA
 GGCTTATACA TTTTTATATC AGCTTTCAGA GTAACCAGGC TAAGTACATT TTTTCCTTAA
 AAGGGAAACC TTTAATGAAA ATATCTTAGG CTAAGTTAGT GGTAAAATTA CCTCCATTAT

  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:  rs809721 maps exactly once on NCBI human chromosome 14
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
14NW_925539.13254206332599941minusAalt_assembly_1CeleraCeleraview300
14NW_001838111.11159367732892687minusAalt_assembly_8HuRefHuRefview300
14NT_026437.113373176951801769minusGref_assemblyreferencereferenceview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_026437 AL355833 AL365475 AL365475.1
dbSNP Blast Analysis
GenBank HTGS Finished:
AL355833.4 AL365475.1

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/T
T/T
HWPC
T
ss43571100HapMap-CEUEuropean 120IG 0.300 0.400 0.300 0.500 0.500
HapMap-HCBAsian 90IG 0.778 0.222 0.889 0.111
HapMap-JPTAsian 88IG 0.727 0.205 0.068 0.830 0.170

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.408+/-0.19418015000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwith2hitwithHapMapFreq
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .