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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs2233546          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:98/130
Map to Genome Build:36.3
Citation: PubMed
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:C
Clinical Association:unknown
HGVS Names
NM_006189.1:c.76C>T
NP_006180.1:p.Arg26Trp
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 ss48408068 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs2233546 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
ss3180981GENAISSANCE|GEN2664fwd/BC/Tgtcctggaccagggcctgaccaggcagatgggctacgcgtggagagcctgaagcagcgcg07/19/0110/10/0398Genomicunknown
ss48408068APPLERA_GI|hCV15946318byFreqfwd/BC/Tgtcctggaccagggcctgaccaggcagatgggctacgcgtggagagcctgaagcagcgcg09/28/0511/03/06126Genomicunknown
ss1106844761000GENOMES|CEU.trio.12.15.2008_2573935_chr11_76491609fwd/BC/Tgtcctggaccagggcctgaccaggcagatgggctacgcgtggagagcctgaagcagcgcg12/15/0812/17/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs2233546|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 TTATCGCTTC TGCGGGGACT GGAGTGGAGG CAGATGGGGA CTCCCACCCC TGACACACAC
 CCCATTTTGA GAACTGAGTG GGGCTGGGAA GAGCCAGTGG CAAAGGGAGG GGAAGAGGGA
 AGGGCAGAAA GTAGGTGGGG CCCCCCTTTG GTGGCCTCTT CTCTCCACGG CCCCAGGCTC
 CAGCCCACTT GGGTCCTTGG CGTTGGTGGC AGCAGCACTT GGGCCATGGC GGAGGACAGG
 CCGCAGCAGC CGCAGCTGGA CATGCCGCTG GTCCTGGACC AGGGCCTGAC CAGGCAGATG
 Y
 GGCTACGCGT GGAGAGCCTG AAGCAGCGCG GGGAGAAGCG CCAGGATGGG GAGAAGCTGC
 TGCAGCCAGC GGAGTCTGTG TACCGCCTCA ACTTCACCCA GCAGCAGCGG CTACAGTTCG
 AGCGCTGGAA TGTCGTGCTG GACAAGCCGG GCAAGGTCAC CATCACAGGC ACCTCGCAGA
 ACTGGACGCC TGACCTCACC AACCTCATGA CACGCCAGCT GCTGGACCCC ACTGCCATCT
 TCTGGCGCAA GGAGGACTCG GATGCCATAG ATTGGAATGA GGCCGACGCC CTGGAGTTTG

  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
U01212.1
dbSNP Blast Analysis
UniGene Cluster ID
534335

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group		 Chrom.
Sample Cnt.
 Source C/C
 C/T
 HWP C
 T
ss48408068 AGI_ASP population multiple 68 IG 0.941 0.059 1.000 0.971 0.029

Summary Average
Het.+/- std err:		 Individual
Count		 Founders
Count		 Individual
Overlap		 Genotype
Conflict
0.057+/-0.159 37 37 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
byClusterbyFreqwithHapMapFreqWith1000GenomeData UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .