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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs3766522          
refSNP ID: rs3766522
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:107/129
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_005399.3:c.156+1882T>A
NT_034400.4:g.182303A>T
Links , Linkout

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 ss11380143 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs3766522 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
ss4952565YUSUKE|IMS-JST120916byFreqfwd/BA/Ttcaaactgtagttctgattgtcgttttgcccttttcctggtagttttgctgagtaacttg08/07/0210/10/03107Genomicunknown
ss11380143WI_SSAHASNP|chr1.NT_034400.2_204921byFreqrev/TA/Tcaagttactcagcaaaactaccaggaaaagggcaaaacgacaatcagaactacagtttga07/03/0310/25/06116Genomicunknown
ss76713546AFFY|AFFY_6_1M_SNP_A-8575061fwd/A/Ttgattgtcgttttgcccttttcctggtagttt08/28/0708/30/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs3766522|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='A/T'|mol=Genomic|build=130
 ATTATTCTTA TCTCTCACCT CAGTCTTGGC ATTTGTGAAT TAAGAAAATT ATTCATATAA
 TTTTCAGATT GTCTGAAAAT CAGATAATTC CTAAGGTCTC ATTTAAGTCT AAAATTTTAT
 AGTTCTCAAT GTAGCCTCTT TACTTCTAAA CTCAACATTT TACTTAAACA TCAAACTGTA
 GTTCTGATTG TCGTTTTGCC
 W
 CTTTTCCTGG TAGTTTTGCT GAGTAACTTG GAGTAAACAA TCTTTCTGCT AGTCAGTTGC
 ATTCATTCCT ACTACAGAAA TGTCATGTCA TAAGTGGAAG GGCTTTCCTC CAAAGCTAGG
 CATATTAATA GTTTGTAGCT TTCAAATTCT AAACTGAAAA TCCTGTCATA AAAGTAACTG
 ACAGAAACAG TGGCAGGGGG

  GeneView back to top
GeneView via analysis of contig annotation: PRKAB2 protein kinase, AMP-activated, beta 2 non-catalytic subunit
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_034400->NM_005399
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_034400->NM_005399->NP_005390182303reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs3766522 maps exactly once on NCBI human chromosome 1
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
1NW_001838511.1170029120054191minusAalt_assembly_8HuRefHuRefview200
1NW_924906.1759554122343161plusTalt_assembly_1CeleraCeleraview200
1NT_034400.4182303145108310minusAref_assemblyreferencereferenceview200

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_034400
dbSNP Blast Analysis
GenBank HTGS Finished:
AL356378.17

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/T
T/T
HWPA
T
ss11380143HapMap-CEUEuropean 120IG 0.050 0.400 0.550 0.655 0.250 0.750
HapMap-HCBAsian 90IG 0.022 0.200 0.778 0.655 0.122 0.878
HapMap-JPTAsian 86IG 0.186 0.814 0.527 0.093 0.907
HapMap-YRISub-Saharan African 120IG 0.233 0.767 0.317 0.117 0.883
ss4952565JBIC-allele 1450AF 0.076 0.923

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.257+/-0.25027021000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwithHapMapFreqUNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .