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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs1010246          
refSNP ID: rs1010246
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: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 ss38535661 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs1010246 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
ss1472909TSC-CSHL|TSC0089654fwd/TA/Gatgaccttggaaagccccaagtcctatggggcaacaggtataaataaacaagcattgaca09/07/0010/10/0386Genomic95 %
ss5165346TSC-CSHL|TSC0423764fwd/TA/Gatgaccttggaaagccccaagtcctatggggcaacaggtataaataaacaagcattgaca09/19/0210/10/03108Genomicunknown
ss12098762WI_SSAHASNP|chr10.NT_030059.10_467945fwd/TA/Gatgaccttggaaagccccaagtcctatggggcaacaggtataaataaacaagcattgaca07/04/0310/10/03116Genomicunknown
ss15590222SC_SNP|NT_030059.11_777913fwd/TA/Gatgaccttggaaagccccaagtcctatggggcaacaggtataaataaacaagcattgaca11/17/0311/22/03120Genomicunknown
ss38535661ABI|hCV172666byFreqfwd/TA/Gatgaccttggaaagccccaagtcctatggggcaacaggtataaataaacaagcattgaca07/15/0511/02/06126Genomicunknown
ss69085047PERLEGEN|PGP02275467byFreqfwd/TA/Gatgaccttggaaagccccaagtcctatggggcaacaggtataaataaacaagcattgaca01/30/0708/14/07127Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs1010246|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 ACAGTGCTAT GCTCTTAACA GGTGCTTTAA AAAAACAGCT CTGTGGAATG ATTGACATTT
 ACATCTCTGA GCAGCTGAGC CTGGCAAGAC CTACCAAAGG GCAAGCAGGA TCCTTATATC
 TTGCAGAATA TCTTGCTAAG GAGAGCTCAG GAGGCAGAAC AGATGGACAC ACCTCAAATT
 CATTCTCTGA TATGACCCGT GCTACACCAA GCACCTACTC TGTGCCAAGC CCTGCATTGA
 AGGCAAGTAT GAGACAGCAG ACAAGGCCAG ATGACCTTGG AAAGCCCCAA GTCCTATGGG
 R
 GCAACAGGTA TAAATAAACA AGCATTGACA TCCATAAAGA ATTCCAACCT TTGAGAGTAA
 CTGTGTGTGA TGATGTGTTC ATAATTTTGA TTGTGGAAAT TATTACACAG TATATACATA
 TAGCAAATCA CATTATATAC CTTGAATACA TACAATTTTT ATTTGTCAAT TATACCTTAA
 TGAAGCTGGG GAAAAAAGCT TTCTTATTTG GGTTGATACA TCATCTTCAG AGTGTGAGCA
 ATAGAATTAT TGCCATAACA TTATTATTAA TAATTAATGA AAATATTTAG TTATTTAAAG

  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:  rs1010246 maps exactly once on NCBI human chromosome 10
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
10NW_001837991.2433449875872606minusCalt_assembly_8HuRefHuRefview300
10NW_924862.190949076019730plusGalt_assembly_1CeleraCeleraview300
10NT_030059.1277791382019377plusGref_assemblyreferencereferenceview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_030059 AL359195.9
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AL359195.24 AL357792.16

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss38535661HapMap-CEUEuropean 120IG 0.050 0.450 0.500 0.343 0.275 0.725
HapMap-HCBAsian 90IG 0.156 0.578 0.267 0.254 0.444 0.556
HapMap-JPTAsian 90IG 0.178 0.378 0.444 0.367 0.633
HapMap-YRISub-Saharan African 120IG 0.017 0.367 0.617 0.273 0.200 0.800
ss69085047HapMap-CEUEuropean 120GF 0.050 0.450 0.500 0.275 0.725
HapMap-HCBAsian 90GF 0.156 0.578 0.267 0.444 0.556
HapMap-JPTAsian 90GF 0.178 0.378 0.444 0.367 0.633
HapMap-YRISub-Saharan African 120GF 0.017 0.367 0.617 0.200 0.800

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.427+/-0.1762702102700

  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 .