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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs12792928          
refSNP ID: rs12792928
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:121/129
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
NT_009237.17:g.4109307T>C
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 ss88443545 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs12792928 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
ss20777190SSAHASNP|WGSA-200403-chr11.chr11.NT_009237.16_4086006fwd/BC/Ttattaggtgatatatatatatatatatataacacacacacacacacatatgtataaaaat03/19/0403/19/04121Genomicunknown
ss88443545BCMHGSC_JDW|JWB-0368401fwd/BC/Ttattaggtgatatatatatatatatatataacacacacacacacacatatgtataaaaat02/26/0802/27/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs12792928|allelePos=251|totalLen=501|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=129
 GATGAAAATA TGATCATGTA TTATTCAAAT TCACCTTTAT AAGACACATA AAATGTACCT
 CCAACTGCAC ATTTTTCTTT AGATGAACTG TATTTGACCC AAGCTGCTTT AGTCCACTTA
 TCTTGACTAT TTCTGAAATC ATAGTTACTC TTCTTTTGGA TTGTTATATC TCCTCTGCTT
 CCTGTATTCT TTTTCTTCAG CATCACTGGC ATTCCCTCTT TATTAGGTGA TATATATATA
 TATATATATA
 Y
 ACACACACAC ACACACATAT GTATAAAAAT TTCTCGCTCA CATCAGCTTT TTCATGTGAT
 AATTAAAATT GAATCTAACT CTGAGGAAAA AAAAGTGTGG ATATAAAACC AGGGTTCCTT
 TTCAGTAATG GGAGAGGCCC AGAAATCCTA GAGATCTTGA GATTCTGAAA TAAGGGCTCA
 AGCCCTACTC TGCCCAGAAA ATAGGCGAAT AATGCTTCTT TGAATCTGCT TGGTCTTGAT
 GCTATAAATG

  GeneView back to top
GeneView via analysis of contig annotation: OR51B4 olfactory receptor, family 51, subfamily B, member 4
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_009237->NM_033179
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_009237->NM_033179->NP_1494194109307reverse3' near gene

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs12792928 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_001838021.19506084981233plusTalt_assembly_8HuRefHuRefview221
11NT_009237.1741093075278642plusTref_assemblyreferencereferenceview221
11NW_925006.19408735440549plusCalt_assembly_1CeleraCeleraview221

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_009237
dbSNP Blast Analysis

  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
with2hit
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .