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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs569705          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:83/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:C
Clinical Association:unknown
HGVS Names
NM_032804.5:c.796C>T
NP_116193.2:p.Pro266Ser
NT_008583.16:g.13116770C>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 ss741010 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs569705 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
ss741010SC_JCM|AL133417.1_124282byFreqfwd/BC/Tttctggtgcgagggagaaccctatccaggtccaaggtcttcccttgaagccactggcgcc07/27/0010/25/0683Genomicunknown
ss3930378SC_JCM|AL353781.4_95816fwd/BC/Tttatggtgcgagggagaaccctattcaggtccaaggtgttaccttgaagccactggcgcc09/25/0110/10/03123Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs569705|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=123
 AAGGGCCTGC CGCCTTCCTG GACATCCTGG CCCCGCCCTA CGACCCGGAC GATGGCCGGG
 ACTGCCACTA TTACCGGGTG CTGGAGCCGG TCAGGCCCAA GGAGGCCTCC AGCTCGGCCT
 GTGACCTGCC TCGAGAGGTG TGGCTCCTGG AGACCCCACA GGCCGATGAC TTCTGGTGCG
 AGGGAGAACC CTATCCAGGT
 Y
 CCAAGGTCTT CCCTTGAAGC CACTGGCGCC CAGGAGCGGT GGGCCGAAGA CGTGCCCTAC
 CCTACCACAA GGGCTGTGTC TCTACCCCCT AGCCTGGGCG TTGGATCTAC TGGAATGAGC
 AGCAGCCGCT TCCTCGGCAG CCTTGGGAAG CACGGGCGAC TGGACAGCAG CCGCCGGGCA
 CGGTTATGGG GGCGGGGTGG

  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
AL353781 AL133417 AL353781
dbSNP Blast Analysis
UniGene Cluster ID
99821

  Population Diversity back to top

Sample AscertainmentGenotypesAlleles
ss# Population Individual
Group		 Chrom.
Sample Cnt.
 Source HWP C
 T
ss741010 CEPH 184 AF 0.990 0.010

Summary Average
Het.+/- std err:		 Individual
Count		 Founders
Count		 Individual
Overlap		 Genotype
Conflict
0.020+/-0.098 0 0 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
byFreq UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .