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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs1891393          
refSNP ID: rs1891393
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:92/129
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

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 ss15876352 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs1891393 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
ss2772221TSC-CSHL|TSC0915791fwd/TA/Gaaaaatgccacttttatgggctacggacacaatagaaaattctcaaaagaagatatacaa01/02/0110/10/0392Genomicunknown
ss6197789SC_JCM|NT_008705.12_15610641rev/BC/Tttgtatatcttcttttgagaattttctattgtgtccgtagcccataaaagtggcattttt01/10/0310/10/03111Genomicunknown
ss15876352SC_SNP|NT_008705.15_402755byFreqrev/BC/Tttgtatatcttcttttgagaattttctattgtgtccgtagcccataaaagtggcattttt11/17/0308/14/07120Genomicunknown
ss39835800ABI|hCV26513586rev/BC/Tttgtatatcttcttttgagaattttctattgtgtccgtagcccataaaagtggcattttt07/16/0507/16/05126Genomicunknown
ss65795908ILLUMINA|Human1-rs1891393fwd/BA/Gaaaaatgccacttttatgggctacggacacaatagaaaattctcaaaagaagatatacaa10/10/0610/10/06127Genomicunknown
ss66302284AFFY|SNP_A-1849562byFreqfwd/TA/Gtatgggctacggacacaatagaaaattctcaa10/29/0608/14/07127Genomicunknown
ss69072810PERLEGEN|PGP04364108byFreqrev/BC/Tttgtatatcttcttttgagaattttctattgtgtccgtagcccataaaagtggcattttt01/30/0708/14/07127Genomicunknown
ss74871901ILLUMINA|ILMN_Human_1M_rs1891393fwd/TA/Gaaaaatgccacttttatgggctacggacacaatagaaaattctcaaaagaagatatacaa08/28/0708/29/07129Genomicunknown
ss75975028AFFY|AFFY_6_1M_SNP_A-1849562fwd/TA/Gtatgggctacggacacaatagaaaattctcaa08/28/0708/29/07130Genomicunknown
ss80866901HGSV|Cor18507_SNV_20070510.chr10_18467436rev/BC/Tttgtatatcttcttttgagaattttctattgtgtccgtagcccataaaagtggcattttt11/26/0711/27/07130Genomicunknown
ss88117561BCMHGSC_JDW|JWB-0244403rev/BC/Tttgtatatcttcttttgagaattttctattgtgtccgtagcccataaaagtggcattttt02/26/0802/27/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs1891393|allelePos=201|totalLen=1126|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 TATATTAAAT TACATGAGAT ACAGTACTTT TCTCCTCAAA GATAAGCATA GACATTTTAA
 ACCTATCATC TCCACCATAG CACTGATTTG CGCCAGGCTT AAAGAATGGG TCTTGATACA
 GTTAAAGATT TAGCCATAAA GCATCATTGA TTTTCCTAAA CTTTGGTATT AAAAATGCCA
 CTTTTATGGG CTACGGACAC
 R
 AATAGAAAAT TCTCAAAAGA AGATATACAA ATGGCCAACA AACATATGAG AAAATGCTCA
 ACATCAATAA TGATCAGGGA AATGCAACTC AAAACCACAA AGTGATACCA CCTTACCCCT
 GTAAGAATGA CCATAATCAA AGAATCAAAA AACAGATGTT GGCATGGATG CAGTGATCAG
 GGAACACTTC TGCACTGCTG GTGGGAATGT AAACTAGTAC AGCCACTATG GAAAACAGTG
 TGGAGATTCC TTAAAGGACT AAAAGTAGAA CTACCATTTG ATGTAGCAAT GCCACTACTG
 GGTATCTACC CAGAGGAAAA GAAGTCATGA TTCAAAAAAT ATACTTGCAC ATGCATGTTT
 ACAGCAGCAC AATTCACAGT AGCAAAATTG TGGAACCAAC CCAAATGCCC ATCAATCAAC
 GAGGTGATAA AGAAACTCTG ATATATATGA TGATGGGATA CTACTCAGCC ATGAAAAGAA
 ATAAATTAAC AGCATTTGCA ATGACCTGGA TGAGATTAGA GACTATTATT CTAAGTGAAG
 TAACTCAGGA ATGGAAAATC GAACATCATA TGTTCTCACT GACATGTGGG AGCTAAGCTA
 TGAGGATGCA AAGGCATAAG AATGATACAA TGGACTTTGG TGACTTGGGG GGAAGTGTGG
 GAGGGGGCAC GGGATAAAAG ACAACAAATA TGGTGCAAGG TATACTGCTA GGTTGATGGG
 TGTACCAGGT TCTCACAAAT CTCCACTAAA GAACTTACTC ATGTAACCGA ATACCACCTG
 TACCCCAATA ACTTATGGAA AAATAAAATT AAAAAAATTA AAATGCCACT TTTATTTAAA
 TTTTGCTGAA TGTTAAACAG CAGCACTTAA ATATTGGTTT GTAATAATTT CTAAAATGGG
 AACATTTTGA ACAGCAACAA TCAGC

  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:  rs1891393 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_001837931.21268916418092813plusAalt_assembly_8HuRefHuRefview200
10NW_924584.11811386518113865minusTalt_assembly_1CeleraCeleraview200
10NT_008705.1540275518467436minusTref_assemblyreferencereferenceview200

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_008705.12
dbSNP Blast Analysis
GenBank HTGS Finished:
AL360231.16 NC_000010.9

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss15876352HapMap-CEUEuropean 120IG 0.483 0.467 0.050 0.717 0.283
HapMap-HCBAsian 90IG 0.378 0.289 0.333 0.522 0.478
HapMap-JPTAsian 90IG 0.356 0.533 0.111 0.622 0.378
HapMap-YRISub-Saharan African 120IG 0.183 0.617 0.200 0.492 0.508
ss66302284HapMap-CEUEuropean 118GF 0.492 0.458 0.051 0.720 0.280
HapMap-HCBAsian 90GF 0.378 0.289 0.333 0.522 0.478
HapMap-JPTAsian 90GF 0.356 0.533 0.111 0.622 0.378
HapMap-YRISub-Saharan African 120GF 0.183 0.617 0.200 0.492 0.508
ss69072810HapMap-CEUEuropean 120GF 0.483 0.467 0.050 0.717 0.283
HapMap-HCBAsian 90GF 0.378 0.289 0.333 0.522 0.478
HapMap-JPTAsian 90GF 0.356 0.533 0.111 0.622 0.378
HapMap-YRISub-Saharan African 120GF 0.183 0.617 0.200 0.492 0.508

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.484+/-0.0892702102700

  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 .