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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs32763325          
refSNP ID: rs32763325
Organism:mouse (Mus musculus)
Molecule Type:Genomic
Created/Updated in build:125/128
Map to Genome Build:37.1
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Strain:not submitted
Ancestral Allele:Not available
Clinical Association:unknown
HGVS Names
Links

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 ss46188433 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs32763325 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
ss46188433ABI|mCV22815540byFreqfwd/TA/Ggtgtacaacattgttctcaaagatttcatggtcacagggccaacgatgtcatctgcctta07/20/0512/22/05125Genomicunknown
ss59908596ENSEMBL|NT_110169.2_73554fwd/TA/Ggtgtacaacattgttctcaaagatttcatggtcacagggccaacgatgtcatctgcctta06/13/0606/13/06127Genomicunknown
ss61077534PERLEGEN|NES16048669fwd/TA/Ggtgtacaacattgttctcaaagatttcatggtcacagggccaacgatgtcatctgcctta06/22/0606/22/06127Genomic100 %

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs32763325|allelePos=301|totalLen=601|taxid=10090|snpclass=1|alleles='A/G'|mol=Genomic|build=127
 CTCTGTACCT ATAAGTAAGC CCACGTCTAT ACATAAGTAA CCACCAATAA AAAGTCATTG
 GCTCATCACC ACTTAGACTT TGGTAATATT CTTAGTTTGC TCTGTCATTT GGTCTCTACT
 TGGAGTGAGT AGACATTTGT TCACATCTCC CCCAGAATCG CACCATATAA CATCAAGACC
 TGGAATCCTT ACCTCATCAC CATATCGGCG ATAGCTCACT TCATATAGCA CAATCAGACC
 ATTAGGTTCC TTTGGCTCTT GCCACATTAA GTGTACAACA TTGTTCTCAA AGATTTCATG
 R
 GTCACAGGGC CAACGATGTC ATCTGCCTTA GCTATAAAAA GCAAGTAAAG GGTCAAATAT
 AACTCTTGAA TCAAATTCTA TTGCAGCCAC CAACATCTAA AAAGACCTGG TTAAAGCTGG
 CTATGTAATT TTTCCATGTC TTATTTTCTT CCGCAGAAAA TGTAAAACTC ATGGAGTAAG
 AAGATACCTC AGTCAGTAAA ACCTGAGTTC AATCCTTAGA ATCCACACAA AAGAGCTGAA
 ACATAGTGTT CTAAGAATCC CAATGTAGAA AAGACGGAGA CAAGCAGATC CCTCAAACTC

  GeneView back to top
GeneView via analysis of contig annotation: Insr insulin receptor
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
CeleraNW_001030882->NM_010568
function
C57BL/6JNT_039455->NM_010568
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
CeleraNW_001030882->NM_010568->NP_034698100149reversemissenseCPro [P]2838
contig referenceTLeu [L]2838
C57BL/6JNT_039455->NM_010568->NP_034698173588reversesynonymousCThr [T]3848
contig referenceTThr [T]3848

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs32763325 maps exactly once on NCBI mouse chromosome 8
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
8NT_039455.71735883173588plusAref_strainC57BL/6JC57BL/6Jview300
8NW_001030882.11001493399525plusAalt_assembly_1CeleraCeleraview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_110169.2
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AC168068.3 AC087150.1 AC087153.1
3D structure mapping
NP_034698  

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
G/G
ss46188433CRAMUS_MOUSE 10IG 3 2
ss61077534MM_PANEL2 30IG 13 2

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
-1.000+/-0171730

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

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Revised: May 25, 2006 1:38 PM .