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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs8022282          
refSNP ID: rs8022282
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:116/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:C
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 ss40417693 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs8022282 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
ss12305883WI_SSAHASNP|chr14.NT_026437.10_86649182fwd/BC/Tcctggaaatgtttaatgagttgcttgaagagtgtgtgctaatggtgtgagagtgtgaaac07/04/0310/10/03116Genomicunknown
ss21225079SSAHASNP|WGSA-200403-chr14.chr14.NT_026437.10_86649182fwd/BC/Tcctggaaatgtttaatgagttgcttgaagagtgtgtgctaatggtgtgagagtgtgaaac03/19/0403/19/04121Genomicunknown
ss40417693ABI|hCV29283934fwd/BC/Tcctggaaatgtttaatgagttgcttgaagagtgtgtgctaatggtgtgagagtgtgaaac07/17/0507/17/05126Genomicunknown
ss78775614HGSV|Cor12878_SNV_20070510.chr14_105818551fwd/BC/Tcctggaaatgtttaatgagttgcttgaagagtgtgtgctaatggtgtgagagtgtgaaac10/17/0710/20/07129Genomicunknown
ss90073828BCMHGSC_JDW|JWB-0823806fwd/BC/Tcctggaaatgtttaatgagttgcttgaagagtgtgtgctaatggtgtgagagtgtgaaac02/26/0802/29/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs8022282|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 TTGTCTTAGT TTCTGAATTT TATTTAGAAA TCAGATACTA AGCGTTAGAA TGTAAAAATT
 GAGAAAATGA TATTATTCTG ACCTCGTTAA CAAAAAACAT GAAGAATTAC AAAAAATAAA
 CCCCTCACCA TATCTGAGTT GATGTCACAG AGAAAAAAAT CCCTGAAATA TGAGAAAATA
 GGGGCCCGCA GAGAGAACTA GGGTGCGTTT ATTAGAGTAC CTGGGGCAGG TGCCACTCAT
 GGCATGGTAT TGAAGATAGG AAAAAGCTAA CCTGGAAATG TTTAATGAGT TGCTTGAAGA
 Y
 GTGTGTGCTA ATGGTGTGAG AGTGTGAAAC TCCTGGCACT TGCAGGCTTT TCCTACAGAA
 TTGGGGAAAT CCCCAGACAA CTCACCCACC TGCTGTCCTG TGGTGTTGAC TGGGGAGGAA
 GAACAGTAGC TCCGTTCAAT GCTGAATCCC CCTTCATTAT ATGCAGGAGA CATTTATTAA
 ATCTTGTGTC CTGTGGGCAC TGGTAGAATC AACTAGAACA CAAGGAAACA GAGGACATCA
 GGGAAACTCT ACCCAGAATC ACCTCCCGTC TGTTTCCTGA GGAATGAAAT CCAGAATCTG

  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:  rs8022282 maps exactly once on NCBI human chromosome 14
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
14NW_925561.15343253186678001plusCalt_assembly_1CeleraCeleraview300
14NW_001838121.158990286888497plusTalt_assembly_8HuRefHuRefview300
14NT_026437.1187748551105818551plusCref_assemblyreferencereferenceview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_026437
dbSNP Blast Analysis

  Population Diversity back to top
There is no frequency data.

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterwith2hit
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .