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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs10929536          
refSNP ID: rs10929536
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:120/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:A
Clinical Association:unknown
HGVS Names
Links

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 ss16856752 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs10929536 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
ss16856752CSHL-HAPMAP|CSHL-HuAA-200402.chr2.NT_005334.14_3542657byFreqfwd/TA/Gtgatggacacaaaatggatactctatgccaatgattgacagaaagaacaggcccactcac02/17/0410/26/06120Genomicunknown
ss20102458CSHL-HAPMAP|CSHL-HuFF-200402.chr2.NT_005334.14_3542657fwd/TA/Gtgatggacacaaaatggatactctatgccaatgattgacagaaagaacaggcccactcac02/21/0403/04/04120Genomicunknown
ss21617337SSAHASNP|WGSA-200403-chr2.chr2.NT_005334.14_3542657fwd/TA/Gtgatggacacaaaatggatactctatgccaatgattgacagaaagaacaggcccactcac03/20/0403/20/04121Genomicunknown
ss44289101ABI|hCV3041796fwd/TA/Gtgatggacacaaaatggatactctatgccaatgattgacagaaagaacaggcccactcac07/18/0507/18/05126Genomicunknown
ss77413801HGSV|Cor12156_SNV_20070510.chr2_8659120fwd/TA/Gtgatggacacaaaatggatactctatgccaatgattgacagaaagaacaggcccactcac10/09/0710/12/07129Genomicunknown
ss91048889BCMHGSC_JDW|JWB-1197795fwd/TA/Gtgatggacacaaaatggatactctatgccaatgattgacagaaagaacaggcccactcac02/26/0803/01/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs10929536|allelePos=279|totalLen=779|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 CTGCAGCCCT CCTGGCCTCT GGGCTCACTG TTAGTAGTGG ATGTGTCTTC TCCATTTCTG
 ATTGCCTAGT GCTTGGCCTG GTGCCTGGAA TATGCTAGAT GCCCAATAAT ATGGACTGAA
 TCACAGCAAA AAGGGAGGGA GGGAGGAAGT AGGTGGATAG GTTTGATGGA AAAATGAGCA
 CTCACATCAA GCAAGATGCT GAGGTGTGAT CTATGTTGGT AACATTATAT AAGGCTTGCA
 CTTGCCTATG ATGGACACAA AATGGATACT CTATGCCA
 R
 ATGATTGACA GAAAGAACAG GCCCACTCAC GTGGCTTTAT GCATTTCTGT AGCTCCACAG
 GGTCGAGACC CCTACCTTGC CTATGGCGGT CTTCTAGAAC CAGAGAAACC TCTGGATATT
 TGAAAGACAT AAGGGGCtgt gttggtaaat tttatgtgtc aacttggctg agtcaccatg
 cccagatatt tggtcaaaca ttattctcga tgtttctgtg agggtgcctt tgactgagat
 tgatatttaa atcagtggac tttgagtaaa gcaggtgacc ttccatcgtg tgtgtgggtc
 tcacccaatc aggttaaggc ctgaagaggc taaagagtga ccttccccga gcaagaagga
 atcctgccag gcctctgggc ttgaaccaca gccccaaact ttcccaatct gcatcctgct
 ggccagcctg cagattttct ggaatttaca caattccgta attttgtaag ccaaatcctt
 aaaataaatc tctctatata

  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:  rs10929536 maps exactly once on NCBI human chromosome 2
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
2NW_001838766.17997088554578plusGalt_assembly_8HuRefHuRefview278
2NW_927719.185527458620810plusAalt_assembly_1CeleraCeleraview278
2NT_005334.1535426578625973plusAref_assemblyreferencereferenceview278

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_005334
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
ss16856752HapMap-CEUEuropean 120IG 0.150 0.567 0.283 0.251 0.433 0.567
HapMap-HCBAsian 90IG 0.489 0.422 0.089 1.000 0.700 0.300
HapMap-JPTAsian 88IG 0.341 0.386 0.273 0.150 0.534 0.466
HapMap-YRISub-Saharan African 120IG 0.917 0.083 0.752 0.958 0.042

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.447+/-0.15427021000

  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 .