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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs17880808          
refSNP ID: rs17880808
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:124/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:A
Clinical Association:unknown
HGVS Names
NM_003150.3:c.372+108A>G
NM_139276.2:c.372+108A>G
NM_213662.1:c.372+108A>G
NT_010755.15:g.4221765T>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 ss69380276 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs17880808 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
ss28526937PGA-UW-FHCRC|STAT3-045048fwd/TA/Gagatctactaaaaaagaaggaaaagaaattaatagatcaataatcataaaaatacattga11/05/0411/05/04124Genomicunknown
ss69380276SI_EXO|NT_010755.15_4221765rev/BC/Ttcaatgtatttttatgattattgatctattaatttcttttccttcttttttagtagatct04/12/0704/12/07127Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs17880808|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=127
 TACAGAAATA GTAACGACCT CCCCTTCGCC CCCCGCCGAC AGAGAGCCTT CACCCAGGCT
 CTGAAGCCTT TGTTCCGTTG TTTCCTAGAA TAAATGCTTT CCTTGATGAA TACATTAGTT
 TTAAGGTGCC ACAGTTCAGT CCACATCTCC ATGGTCTGCT GCTGATTTTT ATTCTCTTTC
 TCTCCTACTT ATAGAGCAGG TATCTTGAGA AGCCAATGGA GATTGCCCGG ATTGTGGCCC
 GGTGCCTGTG GGAAGAATCA CGCCTTCTAC AGACTGCAGC CACTGCGGCC CAGGTGAGAC
 CTGAGACAAA ACAAATCCCT GGTCTGGGAG GAATGGAAAA TCAAACAACT TTATAATGAG
 ATAAATTATT AGATCTACTA AAAAAGAAGG AAAAGAAATT
 R
 AATAGATCAA TAATCATAAA AATACATTGA AAAACTCTAA AAAAAAAGAA AGTTCCACCC
 CCCAAAATAC ATTGAAAAAC TCTAAAAAAA AGAAAGTTCC ACCAAAAGAA TCCAACAGAC
 CCAATGGTTT AAAAGTTTTG TTTTGTTCTG ACAAATTTTC TTTGTTTTTC TTTTTTTTTT
 TTTCTGAGAC AGAGTTTTGC TCTTGTTACC CAGGCTAGAG TGCAATGGCG CGATCTTGGC
 TCACTGCAAC CTCCACCTCC AGGGTTCAAG TGATTCTCCT GCCTCAGCCT CAAGAGTAGC
 TGGGATTATA GGCGTGTGCC ACCACACCCA GCTAATTTTG TATTTTTAGT AGAGACGGGG
 TTTCTTCATG TTGGTCAGGC TGGTCTCGAA CTCCTGACCT

  GeneView back to top
GeneView via analysis of contig annotation: STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
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_010755->NM_003150
function
referenceNT_010755->NM_139276
function
referenceNT_010755->NM_213662
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_010755->NM_003150->NP_0031414221765reverseintron
referenceNT_010755->NM_139276->NP_6448054221765reverseintron
referenceNT_010755->NM_213662->NP_9988274221765reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs17880808 maps exactly once on NCBI human chromosome 17
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
17NW_001838436.290178536261940plusAalt_assembly_8HuRefHuRefview400
17NW_926828.1402298437151793minusTalt_assembly_1CeleraCeleraview400
17NT_010755.15422176537750995minusTref_assemblyreferencereferenceview400

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_010755.15
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
HWPA
G
ss28526937PGA-AFRICAN-PANELAfrican American 48IG 1.000 1.000
PGA-EUROPEAN-PANELEuropean 46IG 0.957 0.043 1.000 0.978 0.022

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.021+/-0.100472600

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

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Revised: May 25, 2006 1:38 PM .