Skip to main content
NCBI
 dbSNP
PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM Books SNP
Search for SNP on NCBI Reference Assembly
transparent GIF
Spacer gif
BUILD 130
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Reference SNP(refSNP) Cluster Report: rs8177445          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:117/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:T
Clinical Association:unknown
HGVS Names
NM_002084.3:c.382T>C
NP_002075.2:p.Phe128Leu
NT_029289.10:g.11569951T>C
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 ss8820639 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs8177445 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
ss8820639EGP_SNPS|GPX3-008983fwd/BC/Tctcaacaggtatgtccgaccaggtggaggcttgtccctaatttccagctctttgagaaag06/05/0301/23/04117Genomicunknown
ss74899345ILLUMINA|ILMN_Human_1M_rs8177445fwd/BC/Tctcaacaggtatgtccgaccaggtggaggcttgtccctaatttccagctctttgagaaag08/28/0708/29/07129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs8177445|allelePos=256|totalLen=511|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
 ATGTGCATCC GCAGGGAGCA CCAAGGTTGA GGGACACTGA AAAGGGACCA GGCTAGAAAG
 GAAGACCGTG GACTCACATT ATGCCTATGC CCACTGCACA TTCACTGGCT CCTGCTGCCC
 ACTGCAGAAT AAATCCAGAC TCCCAACACC CTCTCCCCTG TTCTGTCCCT TCCTCTCATT
 TCTGAGCCCT GTGCCCACCT CCTTGGGACC CACCTAAGAA CATTTCTCAA CAGGTATGTC
 CGACCAGGTG GAGGC
 Y
 TTGTCCCTAA TTTCCAGCTC TTTGAGAAAG GGGATGTCAA TGGAGAGAAA GAGCAGAAAT
 TCTACACTTT CCTAAAGGTA AGTGAGCTGC CACCTGTGCT GGCTGGGGCT GCAGCCCCTC
 CTGGCTCCAG CCCACAGCGT CAGGGCCCAT GCCACCTCCC CTGCTCCTGG GCTCTTGGGG
 AATTTCTTGG CACCTGACTA TTGTTCCAAC TAGAGGGCTC TGCAGACCCT GACTAGGGTC
 TCATTGGCCC ATTTT

  GeneView back to top

GeneView via analysis of contig annotation:  

View more variation on this gene (click to hide).
Include clinically associated: in gene region cSNP has frequency double hit
Assembly SNP to Chr Chr Chr position Contig Contig position Allele
Function mRNA Protein
mRNA to Chr Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via analysis of contig annotation: N/A.

GeneView via direct blast against RefSeq sequences (used when no gene model is available):

Function Chr mRNA Protein
SNP to mRNA Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Integrated Maps: back to top
Genome Build Chr Chr Pos Contig Contig Pos SNP to
Chr		 Contig
allele		 Group term Group label Contig label Neighbor
SNP		 Map Method
doesn't map to any assembly.

  NCBI Resource Links back to top
Resource
Submitter-Referenced
GenBank
AY310878
dbSNP Blast Analysis
UniGene Cluster ID
386793

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group		 Chrom.
Sample Cnt.
 Source C/T
 T/T
 HWP C
 T
ss8820639 PDR90 Global 168 IG 0.012 0.988 1.000 0.006 0.994
HapMap-CEU European 120 IG 1.000 1.000
HapMap-HCB Asian 90 IG 1.000 1.000
HapMap-JPT Asian 90 IG 1.000 1.000
HapMap-YRI Sub-Saharan African 120 IG 1.000 1.000

Summary Average
Het.+/- std err:		 Individual
Count		 Founders
Count		 Individual
Overlap		 Genotype
Conflict
0.003+/-0.041 615 499 0 0

  Validation Summary: back to top
Validation status Marker displays
Mendelian segregation		 PCR results confirmed
in multiple reactions		 Homozygotes detected
in individual genotype data
byClusterwithHapMapFreq UNKNOWN UNKNOWN YES

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
HAPLOTYPE:Submission | Specifications | Sample HapSet | Sample Individual
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement

Revised: May 25, 2006 1:38 PM .