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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs2945496          
refSNP ID: rs2945496
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:101/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:Not available
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 ss4152260 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs2945496 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
ss4152260SC_JCM|AC068152.3_48085fwd/TA/Gtctggttccataaccagaaattgctacctgctcttctaatagaatggagggcttttccat10/15/0110/10/03101Genomicunknown
ss75322060ILLUMINA|ILMN_Human_1M_rs2945496fwd/TA/Gtctggttccataaccagaaattgctacctgctcttctaatagaatggagggcttttccat08/28/0708/29/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs2945496|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129
 AGTGATAATT TCTTCATATA GTGCAAAGTA GTTTGTAAGG TGGTTTTAAA TTCATGAGGT
 CTCAAGTACT CTCTGCCTTA TAGGACAGAT GTAGATACGG TTTCGGTTTT TCTGTTTTTA
 CAGTTTTATA AGAGTACAAG TGATGCTGTT TTATTTGAAG CCTGAGAGCT TCTGGTTCCA
 TAACCAGAAA TTGCTACCTG
 R
 CTCTTCTAAT AGAATGGAGG GCTTTTCCAT TCTTAGACCA TCCAACTCTG AACTTGCTCT
 GAATCTCAAA CCTTTCTGTT CACAGAACAA ATGCTCAAGG GCTTTCAAGA GTGTTTCTGT
 AGATTAGGTT TATTAGCATC AACTTCATGA CTTCTAAAAT GTGACTACTT TCATGTCCAG
 ATAGCTTGAA TACAGGTATC

  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:  rs2945496 maps exactly once on NCBI human chromosome 17
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
17NW_001838448.137139240503412plusGalt_assembly_8HuRefHuRefview200
17NW_926883.134831441575155plusGalt_assembly_1CeleraCeleraview200
17NT_010783.14377842042480141plusGref_assemblyreferencereferenceview200

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
AC068152 AC069007 AC091132
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
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .