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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs9826151          
refSNP ID: rs9826151
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:119/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/T
Ancestral Allele:T
Clinical Association:unknown
HGVS Names
NM_002577.3:c.188-2572T>A
NT_029928.12:g.1145960T>A
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 ss13658860 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs9826151 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
ss13658860BCM_SSAHASNP|chr3.NT_029928.11_1145960fwd/BA/Ttctgatgaaacagtgtgcgctctgcactgaaactactgctctgtttctaagtgtccccca11/05/0311/22/03119Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs9826151|allelePos=501|totalLen=1001|taxid=9606|snpclass=1|alleles='A/T'|mol=Genomic|build=119
 AAGTGTtcag caaacttgga atagaagaga atgcccttta gcctcataaa ggacatcttt
 taaaaaccta ccattggcat taaacttaag ggtaaaaaga atgacagttt ttcctcttag
 atcaggaaaa ataaaatttc tcttcatcca cttttattca acaatgtact gaagggtcta
 gctaatgtag taaggcaaaa aaaaattttt tttaagaaaa cgaataaaag gaatccagat
 tggaaagaag taaacttgat tttattcacc gacaacatga ttgaattttt gtagcaaaat
 tgtatattta caaaaatact agtggaagta agtgtaataa ggtttcagga tataagatta
 gtattcaaga aacaactgtg tttctttatg gctgcaatga atgattaaaa agggaattTT
 AAAACTGCCA TTTGCAATAG TATCAAAACC AGGAAATACC GAGGCAGAAA TCTGATGAAA
 CAGTGTGCGC TCTGCACTGA
 W
 AACTACtgct ctgtttctaa gtgtccccca gagttcatgt gttagaaact gaagccccag
 taagagagtg ttgagacatg ggaccttcaa gaggcgacgc gagtgctcac ggatggactc
 atgtctttat tgtggatgcg agttgcttat aaaagccagt ttggccctct cctgctctct
 ttcttgcaat gtgatgcctt cggctacgtt atgacacaac aagaaggacc ctcaccaggt
 gtggcttctt ggtccttgac ctggaggact ttccagcctc caggagaact gtgagccaaa
 tgaaCtttta tttttttgag gcagtctcac gctgtgactc aggctgggga gtgcagtgac
 acaatctcgg ctcactgcag cctccacctc ctgggttcaa gcaattcttg tgccGctata
 ctcggctgaa gtttgcattt tagatacagt gttttgccat gttggccaga tgggtcttga
 actcctggcc ttatgtgatc

  GeneView back to top
GeneView via analysis of contig annotation: PAK2 p21 protein (Cdc42/Rac)-activated kinase 2
View variations for gene:
Include clinically associated: in gene region cSNP has frequency double hit
Group
Label
Contig->mRNAGene Model (contig mRNA transcript) Color Legend
referenceNT_029928->NM_002577
function
HuRefNW_001838889->NM_002577
function
CeleraNW_921873->NM_002577
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_029928->NM_002577->NP_0025681145960forwardintron
HuRefNW_001838889->NM_002577->NP_002568854373forwardintron
CeleraNW_921873->NM_002577->NP_002568788813forwardintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs9826151 maps exactly once on NCBI human chromosome 3
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
3NW_001838889.1854373193822622plusTalt_assembly_8HuRefHuRefview500
3NW_921873.1788813195107333plusTalt_assembly_1CeleraCeleraview500
3NT_029928.121145960198010623plusTref_assemblyreferencereferenceview500

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_029928
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 .