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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs11228206          
refSNP ID: rs11228206
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:120/129
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_002335.2:c.91+16990C>T
NT_033903.7:g.13403058C>T
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 ss18490596 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs11228206 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
ss16217390SC_SNP|NT_033903.6_13270305fwd/BC/Tccccactgactgacacccctgagtcagtctcaccctggaactgtttctctcactatttgc11/18/0311/22/03120Genomicunknown
ss18490596SC_SNP|SC-CHR9-12_NA11321-200402.chr11.NT_033903.6_13270305fwd/BC/Tccccactgactgacacccctgagtcagtctcaccctggaactgtttctctcactatttgc02/20/0403/04/04120Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs11228206|allelePos=255|totalLen=455|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=120
 AGTAAGTGCA AGCCCTCCTT GTCATCCCAG ACCTCAGCCT GCCCATTTAA TGGATGAAGA
 CACTGAGGCC TGGAGGGAAC AGTGACTTCG GAGCCACTCT CCTGGACTCT GCCACTCCTC
 TCGCCTCCCA TATGAACCTG AGTGGCCACA TGACCCTGGG GGAGAGCTAC TCAACTGTCC
 CAAGGAGAGG GTGATGACTG CTGGCCTCCC ACCGGCCATC AGCGCCCCAC TGACTGACAC
 CCCTGAGTCA GTCT
 Y
 CACCCTGGAA CTGTTTCTCT CACTATTTGC CATGGCCTTG GGCCGCTTCC GGGGGCTTGG
 CAAGGCAGGA GGCGTGGAAC CAAGATGGTA TGTAATCAGA ATGCTATATT TTGTTGAAAA
 TAAGAATGTT AGTAATGGGC TGGTTTCTGG CAGGTCAAAC TGGGACTCTG AAATACATAT
 TTTTCTCTGC TCTGCCCTAA

  GeneView back to top
GeneView via analysis of contig annotation: LRP5 low density lipoprotein receptor-related protein 5
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_033903->NM_002335
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_033903->NM_002335->NP_00232613403058forwardintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs11228206 maps exactly once on NCBI human chromosome 11
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
11NW_001838025.296993364432952minusGalt_assembly_8HuRefHuRefview254
11NW_925106.11378017865432102plusCalt_assembly_1CeleraCeleraview254
11NT_033903.71340305867853839plusCref_assemblyreferencereferenceview254

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_033903
dbSNP Blast Analysis
GenBank HTGS Finished:
AP000807.4 AP002366.4

  Population Diversity back to top
There is no frequency data.

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

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Revised: May 25, 2006 1:38 PM .