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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs35453148          
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:A/G
Ancestral Allele:Not available
Clinical Association:unknown
HGVS Names
NM_014475.3:c.598G>A
NP_055290.1:p.Val200Met
NT_011109.15:g.21711127G>A
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 ss48293996 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs35453148 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
ss48293996SNP500CANCER|DHDH-06byFreqfwd/TA/Gggagggcagaagccagagaagatttcygtctgggaaggcgtcatgaaacaggtaccatct08/19/0511/03/06126Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs35453148|allelePos=72|totalLen=300|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=126
 ACATCGGCAT CTACTGTGTC CAGTTCACCT CCATGGTCTT TGGAGGGCAG AAGCCAGAGA
 AGATTTCYGT C
 R
 TGGGAAGGCG TCATGAAACA GGTACCATCT ATCCTGGAAT ATTTCATGGT GATGGGAATG
 ATTCTGTCTC TCTGGGAGCA CTGAACTGAG GACAAGTCTC CAAGTCAATG AGAATTAGAT
 CARACACCTA GAGGAACAAC TTTCCATGAA GCCAGAGAGG ATCAGAGTCA AGACTGCAGG
 TGGGCACTCT CCTGGGACTT TGCTGTGTGA TCTTAGCCAG CAGACTTA

  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_011109
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss# Population Individual
Group
Chrom.
Sample Cnt.
Source A/G
G/G
HWP A
G
ss48293996 P1 202 AF 0.030 0.970 1.000 0.015 0.985
CAUC1 60 AF 1.000 1.000
AFR1 48 AF 0.125 0.875 0.752 0.063 0.937
HISP1 46 AF 1.000 1.000
PAC1 48 AF 1.000 1.000

Summary Average
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.029+/-0.118 0 0 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
byFreq UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .