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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs5915749          
refSNP ID: rs5915749
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:114/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:G/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 ss8189867 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs5915749 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
ss8189867SC_SNP|NT_011649.11_713828byFreqfwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt04/16/0310/25/06114Genomicunknown
ss8540318SC_SNP|NT_011812.12_455224fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt05/23/0310/10/03117Genomicunknown
ss12026098WI_SSAHASNP|chrX.NT_011812.12_455224fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt07/04/0310/10/03117Genomicunknown
ss19815020CSHL-HAPMAP|CSHL-HuDD-200402.chrX.NT_011757.13_455224fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt02/20/0403/04/04120Genomicunknown
ss20977876SSAHASNP|WGSA-200403-chrX.chrX.NT_011757.13_455224fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt03/19/0403/19/04121Genomicunknown
ss24228126PERLEGEN|afd3856991byFreqfwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt08/10/0409/13/04123Genomicunknown
ss43554166ABI|hCV30246820fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt07/18/0507/18/05126Genomicunknown
ss76844382AFFY|AFFY_6_1M_SNP_A-8706036fwd/BG/Tgcattatctcgcttcacttttgtagaaatcta08/28/0708/30/07130Genomicunknown
ss83392043HGSV|Cor18555_SNV_20070510.chrX_4248316fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt11/27/0712/04/07130Genomicunknown
ss84183815HGSV|Cor19240_SNV_20070510.chrX_4248316fwd/BG/Tctagacaatttgtagcattatctcgcttcacttttgtagaaatctattaacattttattt11/30/0712/06/07130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs5915749|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=130
 AATAAGATAT GCTTGTTGAC TCTGCCAAAT GGAAAGTGGA ACTGATTTCT GGAGGTTTGA
 TCCTAATTCT GGTTTTTTTG GTTGTTGTTG TTTGTTTGTT TGTTTTCCAG GGCAGTATCA
 GATAGTTTCT ATCGGGGGGG CCAAGAAAGA AGTCATTGCA CAATTCTCAA AGCCCATCAT
 TTAAACATGA GTCAATGATC ATTTTTGCAG GGTGAGAATT TGGGAGATTG TTACGGCAGA
 TTGCTCAACC AAGTCAACAC CTCAGCCCAT TTTCATTCTG TCATACATTT CTTGAGAAGG
 AAAAAACGTG TAATTGAAGT GGAGAGATAT ATTTTACGTC AACCCATTTT TACTGTGAGT
 TTATAATCTG CTAGACAATT TGTAGCATTA TCTCGCTTCA
 K
 CTTTTGTAGA AATCTATTAA CATTTTATTT CTTTTTAATC AGTTAATAAA TGGAGGTAGG
 TATAGAGGCA TTCAGAAAAT TAGTCAAAGG TGCAAAGTTA CAGCATGTGA AGACATCAAC
 ATAGGCAGCC CAATATCTTA CCCATAAGCC AAtgacattt tgcatcagat gatttttttt
 tgtggtaggg gccgctcttt gcattgtagg atgatttgca gcatttctgg cctgcacaaa
 ctagatgcca gtagcaatac ctctccctcc ttaaagatgt gacaattggc atgtcttcag
 acagtgtcaa gtgtcattgt gggggATGGG GGGGTGGGCA GGGGTGTAGA AAATACCCCA
 GGTTGATAAT CATTGCATTG GTTCATTCAA GTAGACTAAA

  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:  rs5915749 maps exactly once on NCBI human chromosome X
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
XNW_001842357.18663322262232plusTalt_assembly_8HuRefHuRefview400
XNT_011757.1522703424398580plusGref_assemblyreferencereferenceview400
XNW_927700.130048078606525plusGalt_assembly_1CeleraCeleraview400

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_011812
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
ss24228126AFD_EUR_PANELEuropean 48IG 0.292 0.208 0.500 0.010 0.396 0.604
AFD_AFR_PANELAfrican American 46IG 0.043 0.174 0.783 0.273 0.130 0.870
AFD_CHN_PANELAsian 48IG 0.417 0.333 0.250 0.150 0.583 0.417
ss8189867HapMap-CEUEuropean 120IG 0.350 0.167 0.483 0.100 0.433 0.567
HapMap-HCBAsian 90IG 0.533 0.178 0.289 0.294 0.622 0.378
HapMap-JPTAsian 88IG 0.432 0.159 0.409 0.100 0.511 0.489
HapMap-YRISub-Saharan African 120IG 0.017 0.017 0.967 1.000 0.025 0.975

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.468+/-0.12333226090

  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 .