Skip to main content
NCBI
 dbSNP
PubMed Nucleotide Protein Genome Structure PopSet Taxonomy OMIM Books SNP
Search for SNP on NCBI Reference Assembly
transparent GIF
Spacer gif
BUILD 130
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Reference SNP(refSNP) Cluster Report: rs35762223          
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_182974.2:c.584A>G
NP_892019.2:p.His195Arg
NT_019501.13:g.1424997T>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 ss76891065 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs35762223 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
ss48425238APPLERA_GI|hCV25990961byFreqfwd/BC/Tttcttggtgtttctgaaataccaccaggcgggagctgggccaccaacgggcccagggtct09/28/0511/03/06126Genomicunknown
ss69305907PERLEGEN|PGP17790813byFreqfwd/BC/Tttcttggtgtttctgaaataccaccaggcgggagctgggccaccaacgggcccagggtct01/30/0703/31/08127Genomicunknown
ss76891065SI_EXO|NT_019501.13_1424997fwd/BC/Tttcttggtgtttctgaaataccaccaggcgggagctgggccaccaacgggcccagggtct09/20/0709/20/07129Genomicunknown
ss115815620ILLUMINA-UK|NA18507_000145950_NCBI36.1_chr9_137656011fwd/BC/Tttcttggtgtttctgaaataccaccaggcgggagctgggccaccaacgggcccagggtct01/15/0901/16/09130Genomic99 %

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs35762223|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 CTCATTTATA AGAAATTGCC GTGATTCATT TATTCGTCAT AAACCTCATG GCGTAATTCA
 TAATTTCCTC TGGGAATCAT GTGCGACCTT GACGTATTGG ATCTGTGGAG GAGGAGAAAA
 TGCAAGATCC CAGCTGTATG CTGGTGATAA CAGCTAGGTG GGTTTATTGA GGTAAAAATA
 TTTGTTAAGG TGCTTTTCAT AAGTGCTATT GAGTCCATTT TTGATGTCAT GAATAACTCC
 GTTCAGATAT TCTTTGATGA AGTCTAAAAT ATTATGGGGT GTGCCACCAA CCATCAAGTT
 GCCATAATAG AAATCTCCCT GTCCAAACGG GATGCAAGCT GCTGAGGTCG GCCTCCTCTC
 ATAAGGGAAG TTCTTGGTGT TTCTGAAATA CCACCAGGCG
 Y
 GGAGCTGGGC CACCAACGGG CCCAGGGTCT CCACCCCGAA CTCATTCTGG AAGACCTGGT
 TGGCAGCCAT GCTGAAGAGG AAGTCCACCT CGTCCTGGAT GTGACTGGCG ATGTGTTCAC
 CCAGGCTCTT CACATGCACC AGGGGGCCAT CGAGCCACCA CCTCTCGGTG CCCACTTTAA
 ATGCTTTGAA CGTTCGAAGA GGACTGGGCT CTATGTCAGG CAGCTTGAAG AAGGCGTCCA
 CCATGATGTA GAAGATCACT CGGTAGCCTG TCATGAAGTG CTTATTTGCG GAGTGTAGGA
 ACGGCCTCAG GTACTCCTCT GCAAACCTAG GAAACACACA GTGGGGAAGA AACTTACTTT
 TCTCTTTTTT CTTTTCTTTC TTTTTTTTTT TTTTTTTTTT

  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
GenBank
NT_019501.13
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group		 Chrom.
Sample Cnt.
 Source C/C
 C/T
 T/T
 HWP C
 T
ss48425238 AGI_ASP population multiple 58 IG 0.069 0.276 0.655 0.403 0.207 0.793
ss69305907 HapMap-CEU European 120 GF 0.250 0.750 0.125 0.875
HapMap-HCB Asian 90 GF 0.267 0.733 0.133 0.867
HapMap-JPT Asian 90 GF 0.022 0.356 0.622 0.200 0.800
HapMap-YRI Sub-Saharan African 120 GF 0.017 0.150 0.833 0.092 0.908

Summary Average
Het.+/- std err:		 Individual
Count		 Founders
Count		 Individual
Overlap		 Genotype
Conflict
0.244+/-0.250 305 245 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
byClusterbyFreq UNKNOWN UNKNOWN UNKNOWN

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
HAPLOTYPE:Submission | Specifications | Sample HapSet | Sample Individual
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement

Revised: May 25, 2006 1:38 PM .