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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs35764631          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:126/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Ancestral Allele:Not available
Clinical Association:unknown
HGVS Names
NM_000275.2:c.318G>A
NM_000275.2:c.320A>G
NM_000275.2:c.407G>A
NP_000266.2:p.Arg136Gln
NP_000266.2:p.Glu107Gly
NT_010280.17:g.676114C>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 ss48429577 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs35764631 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
ss48429577APPLERA_GI|hCV25619008fwd/BC/Tccagacacctccctgcttagcaggtatcttgctcccagtcagcagagctgtcttcccaag09/28/0511/30/05126Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs35764631|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=126
 TTTGCAGGAG GTCTTAAATG TCTCCCTAGG CCCAGGTAAA AATAAATCAC CTTGGAGGAA
 AAGTGCAGCC TGGCCAGATG AGACAAAACT CATCCTCTTC TTCACGCTGC TGGTTTGAAA
 GATGGAGGGG CCATGTAGGA CGCGATGTGC GGCCACCGCT GCTGCCAGGG TGGGCACCCC
 AAGTCCGCCT ACCTCAGCTT GGAAAGACGG AGTCGGATGT GCGGGCTGTC CAGAAGGTCT
 CCCTTCTCGG AGGAGGCAGA TGCAGACAGA CCAGACACCT CCCTGCTTAG CAGGTATCTT
 Y
 GCTCCCAGTC AGCAGAGCTG TCTTCCCAAG ACTCTTCAGC AGTGATGAAC TCTGGATGGT
 AAACAGGTAT GCACCGTGAC CTGGAAAGCA AGAGAGGTGT GGTTATCTCT CCTGAAATAG
 TAATGGCTAC AAAGCAAGCT TTCCTCTGAG TTCTGACTGT GTGAAATGGC ACCGAATCAA
 CCCTGGTCTT TCAAAGGACC ACAGACAGTG GTGCACTCTC ATACTGGTGG GAATGGGTTT
 TTTTGTGACC TCTCAGAACA CTTAGGTCAA AGGAAATTTT CTGGAGTCAT TAAAGTCTTC

  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
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group
Chrom.
Sample Cnt.
Source C/C
C/T
HWP C
T
ss48429577 AGI_ASP population multiple 66 IG 0.970 0.030 1.000 0.985 0.015

Summary Average
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.030+/-0.118 38 38 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
UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .