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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs734664          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:86/130
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_015209.2:c.226+70935G>A
NM_201628.2:c.226+70935G>A
NT_004873.16:g.1389492A>G
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 ss16461179 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs734664 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
ss80848TSC-CSHL|TSC0026510byFreqfwd/BC/Taagagtctaagtttttgcctaaaagcaggaggaagaagggaaggaaaaagggaagggaat09/06/0010/25/0686Genomic95 %
ss16461179CSHL-HAPMAP|CSHL-HuAA-200402.chr1.NT_004873.15_1373819rev/TA/Gattcccttccctttttccttcccttcttcctcctgcttttaggcaaaaacttagactctt02/17/0403/04/04120Genomicunknown
ss20599939SSAHASNP|WGSA-200403-chr1.chr1.NT_004873.15_1373819rev/TA/Gattcccttccctttttccttcccttcttcctcctgcttttaggcaaaaacttagactctt03/18/0403/18/04121Genomicunknown
ss41275963ABI|hCV11644275rev/TA/Gattcccttccctttttccttcccttcttcctcctgcttttaggcaaaaacttagactctt07/16/0507/17/05126Genomicunknown
ss82598282HGSV|Cor19240_SNV_20070510.chr1_14741960rev/TA/Gattcccttccctttttccttcccttcttcctcctgcttttaggcaaaaacttagactctt11/30/0712/03/07130Genomicunknown
ss1100871301000GENOMES|NA19240_2008_12_16_18358_chr1_14869241rev/TA/Gattcccttccctttttccttcccttcttcctcctgcttttaggcaaaaacttagactctt12/16/0812/17/08130Genomicunknown
ss118512209ILLUMINA-UK|NA18507_000017124_NCBI36.1_chr1_14869241rev/TA/Gattcccttccctttttccttcccttcttcctcctgcttttaggcaaaaacttagactctt01/21/0901/21/09130Genomic99 %

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs734664|allelePos=501|totalLen=767|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=130
 AATTCTTGGT ATGAATCGGG Ctcatttgga aggcctgttc aaagtaggga tgcccaggcc
 cctccccaga tctactgaat cagaatcaga ggggatgagt tcatggtatc cggggctttc
 acctgctccc caggtaactc tgatgcatac tatcatttga gaatcCTTGA gttctcaaag
 tgtagcccct ggagcagtgg cagcagcatc acctaggtac gtgttaggaa cgtaaatcag
 caggccccac ctcagaccta ctgaagcaga aggtagcaga agctctaggg tgggacccag
 caacctgttt tcaacgaggc ttccaggtgc ctctgaggct cgctcaggct tgaatacccc
 tgCCTTTGAC TAGGAGGACA CAAACACAAA TGCCTTCAGG AGGTGGGCTT GCACCTCTGG
 GGCTGGTAAA GATGAACTAT CTTGTGGGGA GAGAAACTTA TAGTATACTA AAGAGTCTAA
 GTTTTTGCCT AAAAGCAGGA
 Y
 GGAAgaaggg aaggaaaaag ggaagggaat gaaaaagggg aggggagggc tggggaggga
 agggaaggga GAAGACTCTC GGGCCAAATA AAGTATCTAC ATAGACCAGA TCAGCTAGGG
 GCCACCAGTT TGCCATTGTA CAGGGGATGC CATCTTATAT GGCTGTTCTC TTTTAAAGAT
 GACTCCTCAA GTCAATGGTA ATCTTGAGGG CAGATTTGTA CTTCTTGGTA GCCTCTGATA
 GATTGGCGGT ACCCAGGAAA AGTTGG

  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_004873
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotypesAlleles
ss# Population Individual
Group		 Chrom.
Sample Cnt.
 Source HWP C
 T
ss80848 TSC_42_AA 80 AF 0.413 0.587
TSC_42_C 82 AF 0.280 0.720
TSC_42_A 82 AF 0.280 0.720

Summary Average
Het.+/- std err:		 Individual
Count		 Founders
Count		 Individual
Overlap		 Genotype
Conflict
0.438+/-0.165 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
byClusterbyFreqwith2hitwithHapMapFreqWith1000GenomeData
DoubleHit found by:  BCM_SSAHASNP
 UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .