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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs3122257          
refSNP ID: rs3122257
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:103/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
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 ss4367756 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs3122257 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
ss4367756SC_JCM|AL450342.15_116682fwd/BC/Tttagatgcaggttccttaccagatatatgattgcaaatattttctcccattttgtgtttt02/19/0210/10/03103Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs3122257|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=103
 TGTAGCAATT TACTATGCTG CCAGTAGTGG ATAAGAATAT CACTTTCATA GTACCATCAG
 CAGAgagagt cttttcattt gtctattggc catttctata tcttctttgg aaaaatacct
 attcaaattt tttgtcttta ttattgaatt ttaggcattc tttgtatatt ttagatgcag
 gttccttacc agatatatga
 Y
 ttgcaaatat tttctcccat tttgtgtttt tttttttttc tttttcttga tgttacactt
 tgaagctcaa gaatttttaa ttttgacaaa gtcagtttat tatttttttt cttttcttct
 gttttcggga tcatatttaa gaagctaatc taagttcatg aagatttATG TTTCTTCTAA
 GAATTTTATA GCTTTAGCTC

  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:  See all two hits of rs3122257 on the  NCBI human genome map
!WARNING: Several map positions found! The map position is found by blasting with the contig sequences.
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
10NT_035036.215765151015067minusAref_assemblyreferencereferenceview200
10NT_008583.1620083751319688plusTref_assemblyreferencereferenceview200
UnNW_001841023.11743unplacedplusTalt_assembly_8HuRefHuRefview200
UnNW_927934.114937unplacedminusGalt_assembly_1CeleraCeleraview200

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
AL450342 AC037457
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AL450342.16 AL672187.12 NC_000010.9 AC141459.1 AC142442.1 AC142542.1 AC142548.1 AC143350.1 AC143351.1 AC144355.1

  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 .