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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs427832          
refSNP ID: rs427832
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:80/129
Map to Genome Build:36.3
Citation: PubMed
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 ss44385391 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs427832 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
ss566699SC_JCM|AC025155.9_22995rev/BC/Tccagaagaaagccaccagtcaggacgaatcgcatctgtgggttcttgtgtcacatggcgc07/12/0010/10/0380Genomicunknown
ss876268KWOK|OVLP-000804-30597fwd/TA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg09/01/0010/10/0386Genomic99 %
ss1909909KWOK|OVLP-000925-485015fwd/TA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg10/06/0010/10/0387Genomic99 %
ss2181949TSC-CSHL|TSC0557614byFreqfwd/TA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg10/19/0004/07/0488Genomic95 %
ss24295210PERLEGEN|afd2721750byFreqfwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg08/10/0409/13/04123Genomicunknown
ss44385391ABI|hCV950073byFreqfwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg07/18/0511/03/06126Genomicunknown
ss66011960AFFY|SNP_A-1715954fwd/TA/Gatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttct10/26/0610/26/06127Genomicunknown
ss66747647ILLUMINA|HumanHap300v1.1_rs427832fwd/BA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg11/09/0611/09/06127Genomicunknown
ss67323293ILLUMINA|HumanHap550v1.1_rs427832fwd/TA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg11/14/0611/14/06127Genomicunknown
ss67726415ILLUMINA|HumanHap650Yv1.0_rs427832fwd/TA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg11/14/0611/14/06127Genomicunknown
ss70798127ILLUMINA|HumanHap550v3.0__rs427832rev/BC/Tccagaagaaagccaccagtcaggacgaatcgcatctgtgggttcttgtgtcacatggcgc04/20/0703/30/08130Genomicunknown
ss71376564ILLUMINA|HumanHap650Yv3.0_rs427832fwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg04/23/0704/23/07127Genomicunknown
ss75704872ILLUMINA|ILMN_Human_1M_rs427832fwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg08/28/0708/29/07129Genomicunknown
ss79178221ILLUMINA|HumanHap300v2.0_rs427832fwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg04/18/0711/18/07130Genomicunknown
ss82739997HGSV|Cor18555_SNV_20070510.chr3_149949061fwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg11/27/0712/03/07130Genomicunknown
ss83395648HGSV|Cor19240_SNV_20070510.chr3_149949061fwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg11/30/0712/04/07130Genomicunknown
ss83451746KRIBB_YJKIM|KHS464853fwd/TA/Ggcgccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg12/04/0712/05/07130Genomicunknown
ss106305509BGI|BGI_rs427832fwd/TA/Ggcaccatgtgacacaagaacccacagatgcgattcgtcctgactggtggctttcttctgg09/13/0809/15/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs427832|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 AGATGAGAAA TAGGGATCCT GGCTCAACCT CCCAGTGAGT TGGGATTTAT CTCATGGAAC
 TTTTTCCCAA GCTTGATGAA GTTCTGCTGT GCCATATGGA CATGTACAGT TGCTAAATGA
 TAATTTTCCA AAAATAAGCT TCAATTCTCC AAAATGGCAG ATAGAAAGCA GCTGGTGTTA
 CTCAACAGAG ATAAGCCCTC CTAGAGCTCA CCACAGAGAG GAGAGCATCA TGTCTGCAGA
 TGCCACAGCA GATCTGCTGA GAATCAGCCA GCGCCATGTG ACACAAGAAC CCACAGATGC
 R
 GATTCGTCCT GACTGGTGGC TTTCTTCTGG CCATTGCTGT TACAGAGAAG TTTCTAAGCA
 GTACTCAATG CACACAAAAC TAAGTAGAGG CTATATAGGC AATTCTTCAA ATAAGCAATC
 ATTATTCTCA GTAATTCTTG TAGTAAGTGG ATGGTAGGAG GAAAAAAAAA ATACCTTTCC
 ACTGATGATA TCACCTTTAT AGCTATTTCT TGAGTCTCCC TATCTTTTCC ACCTTCTTCA
 AGAAATAGTC CCCTATTACA ATTTGCATGC CCACTCTTGC TGCAGAATTT GTATAGGGGC

  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:  rs427832 maps exactly once on NCBI human chromosome 3
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
3NW_001838884.245590274145838757minusCalt_assembly_8HuRefHuRefview300
3NW_921807.155062401146876731plusAalt_assembly_1CeleraCeleraview300
3NT_005612.1554961509149949053plusGref_assemblyreferencereferenceview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NC_000003.6 AC024991 AC067729.10 AC067729.12
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA
A/A
A/G
G
G/G
N
HWPA
G
N
ss2181949AfAmAfrican American 40IG 0.250 0.500 0.250 1.000 0.500 0.500
CaucasianEuropean 38IG 0.316 0.368 0.316 0.254 0.500 0.500
AsianAsian 40IG 0.600 0.350 0.050 1.000 0.775 0.225
CEPHEuropean 54IG 0.370 0.481 0.148 1.000 0.611 0.389
PDpanelGlobal 46IG 0.217 0.522 0.261 1.000 0.478 0.522
CEPH 184AF 0.500 0.500
CHMJAsian 74IG 0.716 0.270 0.014 0.716 0.270 0.014
ss24295210AFD_EUR_PANELEuropean 48IG 0.292 0.458 0.250 0.752 0.521 0.479
AFD_AFR_PANELAfrican American 46IG 0.217 0.391 0.391 0.371 0.413 0.587
AFD_CHN_PANELAsian 48IG 0.583 0.375 0.042 1.000 0.771 0.229
ss44385391HapMap-CEUEuropean 120IG 0.333 0.483 0.183 1.000 0.575 0.425
HapMap-HCBAsian 90IG 0.489 0.444 0.067 0.343 0.711 0.289
HapMap-JPTAsian 88IG 0.568 0.364 0.068 1.000 0.750 0.250
HapMap-YRISub-Saharan African 120IG 0.117 0.500 0.383 0.371 0.367 0.633
AoD_African_American 90AF 0.440 0.560
AoD_Caucasian 92AF 0.520 0.480
AoD_Chinese 90AF 0.790 0.210
AoD_Japanese 90AF 0.780 0.220

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.485+/-0.090426352320

  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 .