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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs3863292          
refSNP ID: rs3863292
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:108/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
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 ss96392 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs3863292 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
ss90528TSC-CSHL|TSC0109341fwd/TA/Gattcctgactacacatgaagagactgacactaggtgccttacttaggtaggttaagtaat09/06/0010/10/03108Genomicunknown
ss96392TSC-CSHL|TSC0124047byFreqrev/BC/Tattacttaacctacctaagtaaggcacctagtgtcagtctcttcatgtgtagtcaggaat09/06/0003/31/08108Genomicunknown
ss5873189SC_JCM|NT_035080.1_81312rev/BC/Tattacttaacctacctaagtaaggcacctagtgtcagtctcttcatgtgtagtcaggaat01/10/0310/10/03111Genomicunknown
ss10682851BCM_SSAHASNP|chr11.NT_028310.10_4078850rev/BC/Tattacttaacctacctaagtaaggcacctagtgtcagtctcttcatgtgtagtcaggaat06/29/0310/10/03116Genomicunknown
ss23354397PERLEGEN|afd4647994byFreqrev/BC/Tattacttaacctacctaagtaaggcacctagtgtcagtctcttcatgtgtagtcaggaat08/10/0409/13/04123Genomicunknown
ss66366797AFFY|SNP_A-2007246byFreqrev/BC/Tctaagtaaggcacctagtgtcagtctcttcat10/29/0603/31/08127Genomicunknown
ss69307515PERLEGEN|PGP04647994byFreqrev/BC/Tattacttaacctacctaagtaaggcacctagtgtcagtctcttcatgtgtagtcaggaat01/30/0703/31/08127Genomicunknown
ss75127128ILLUMINA|ILMN_Human_1M_rs3863292fwd/TA/Gattcctgactacacatgaagagactgacactaggtgccttacttaggtaggttaagtaat08/28/0708/29/07129Genomicunknown
ss76090277AFFY|AFFY_6_1M_SNP_A-2007246rev/BC/Tctaagtaaggcacctagtgtcagtctcttcat08/28/0708/29/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs3863292|allelePos=165|totalLen=801|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 CTCACCATGA GTTCAGTATA TAATTGTAAC AGAATAAAAA ATCAATTATG TATTCAAGTT
 GCTAGtgtct taagaggttc acatttttat ctaactgatt atcacaaaaa tacttcgagt
 tacttttcat tataattcct gactacacat gaagagactg acac
 R
 taggtgcctt acttaggtag gttaagtaat ttatccaaaa ccacacaATG TAGAACTTAA
 GCTGATTCGG CCATAGAAAC ACAATATGTG GTATAAATGA GACAGAGGGA TTTCTCTCCT
 TCCTATGCTG TCAGATGAAT ACTGAGATAG AATATTTAGT TCATCTATCA CACATTAAAC
 GGGACTTTAC ATTTCTGTCT GTTGAAGATT TGGGTGTGGG GATAACTCAA GGTATCATAT
 CCAAGGGATG GATGAAGGCA GGTGACTCTA ACAGAAAGGG AAAGGATGTT GGCAAGGCTA
 TGTTCATGAA AGTATATGTA AAATCCACAT TAAGCTTCTT TCTGCATGCA TTGGCAATGT
 TTATGAATAA TGTGTATGTA AAAGTGTGCT GTATATTCAA AAGTGTTTCA TGTGCCTAGG
 GGTGTCAAAT ACTTTGAGTT TGTAAGTATA TACTTCTCTG TAATGTGTCT GAATATCTCT
 ATTTACTTGA TTCTCAATAA GTAGGTATCA TAGTGAACAT CTGACAAATG TTTGAGGAAC
 AATTTAGTGT TTACCTATTC ACCAAAATTT ATTAAATGCC TAATCTGTAT CAGATATACA
 ATTATCTGGC GAAATCTGTA ATTCCTAATT TAAACA

  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:  rs3863292 maps exactly once on NCBI human chromosome 11
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
11NW_001838021.19472194977844minusCalt_assembly_8HuRefHuRefview164
11NT_009237.1741059185275253minusCref_assemblyreferencereferenceview164
11NW_925006.19374845437160minusCalt_assembly_1CeleraCeleraview164

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_035080.1
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
ss23354397AFD_EUR_PANELEuropean 44IG 0.182 0.818 0.655 0.091 0.909
AFD_AFR_PANELAfrican American 44IG 0.455 0.545 0.200 0.227 0.773
AFD_CHN_PANELAsian 48IG 1.000 1.000
ss66366797HapMap-CEUEuropean 118GF 0.203 0.797 0.102 0.898
HapMap-HCBAsian 90GF 0.022 0.978 0.011 0.989
HapMap-JPTAsian 90GF 0.111 0.889 0.056 0.944
HapMap-YRISub-Saharan African 120GF 0.150 0.433 0.417 0.367 0.633
ss69307515HapMap-CEUEuropean 120GF 0.200 0.800 0.100 0.900
HapMap-HCBAsian 90GF 0.022 0.978 0.011 0.989
HapMap-JPTAsian 90GF 0.089 0.911 0.044 0.956
HapMap-YRISub-Saharan African 120GF 0.150 0.433 0.417 0.367 0.633
ss96392HapMap-CEUEuropean 120IG 0.200 0.800 0.100 0.900
HapMap-HCBAsian 90IG 0.022 0.978 0.011 0.989
HapMap-JPTAsian 90IG 0.089 0.911 0.044 0.956
HapMap-YRISub-Saharan African 120IG 0.150 0.433 0.417 0.367 0.633
Concordant GenotypeTotal SampleA/AA/GG/G
ss2335439771
ss66366797268
ss69307515269
ss96392269
RefSNP Genotype SummaryTotal IndividualA/AA/GG/G
rs3863292332
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss)GenotypePopulation
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
5212ss96392C/CCSHL-HAPMAPHapMap-JPTNA18965JA18965r23_ch11_JPT_affymetrix:genechip500k
5212ss66366797C/TCSHL-HAPMAPHapMap-JPTNA18965JA18965chr11-HapMap-JPT
5212ss69307515C/CCSHL-HAPMAPHapMap-JPTNA18965JA18965chr11-HapMap-JPT
Genotype data submitted for341 samples from332 individualsIndividual with multiple genotypes submission:270

  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_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .