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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs785448          
refSNP ID: rs785448
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:86/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
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 ss1771810 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs785448 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
ss941333KWOK|OVLP-000804-349919fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc09/01/0010/10/0386Genomic99 %
ss1771810KWOK|OVLP-000925-228520byFreqfwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc10/05/0010/25/0687Genomic99 %
ss2556602SC_JCM|AC069331.3_43059fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc11/03/0010/10/0392Genomicunknown
ss10789395BCM_SSAHASNP|chr15.NT_010194.15_936820fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc06/30/0310/10/03116Genomicunknown
ss17537538CSHL-HAPMAP|CSHL-HuCC-200402.chr15.NT_010194.16_936820fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc02/19/0403/04/04120Genomicunknown
ss21275399SSAHASNP|WGSA-200403-chr15.chr15.NT_010194.16_936820fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc03/19/0403/19/04121Genomicunknown
ss43689386ABI|hCV8717278fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc07/18/0507/18/05126Genomicunknown
ss66219492AFFY|SNP_A-4248508byFreqfwd/TA/Gtagtacacgcaaaaatacatggccagtctctt10/27/0608/14/07127Genomicunknown
ss67840460ILLUMINA|HumanHap550v1.1_rs785448fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc11/14/0611/14/06127Genomicunknown
ss67997223ILLUMINA|HumanHap650Yv1.0_rs785448fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc11/14/0611/15/06127Genomicunknown
ss68288614ILLUMINA|HumanHap250Sv1.0_rs785448fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc12/06/0612/07/06127Genomicunknown
ss69171732PERLEGEN|PGP06193797fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc01/30/0701/30/07127Genomicunknown
ss76365732AFFY|AFFY_6_1M_SNP_A-4248508fwd/TA/Gtagtacacgcaaaaatacatggccagtctctt08/28/0708/30/07129Genomicunknown
ss81077120HGSV|Cor18555_SNV_20070510.chr15_27933555fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc11/27/0711/27/07130Genomicunknown
ss83563104KRIBB_YJKIM|KHS490570fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc12/04/0712/05/07130Genomicunknown
ss84191771HGSV|Cor18517_SNV_20070510.chr15_27933555fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc12/06/0712/06/07130Genomicunknown
ss90106406BCMHGSC_JDW|JWB-0835620fwd/TA/Gtttcacttagtttatagtacacgcaaaaatacatggccagtctcttgccatgttatttcc02/26/0802/29/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs785448|allelePos=201|totalLen=942|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 ACTATTCTGC ATTACATGGG AATAAAATGA TGGGTGGTTT TTTCCGAGAG AACATATCCA
 GGAGCAACGA CGCACCTGCA GTTGGAGCAG ATAGTCGCTA TACTTTCACC GCATCACCAC
 TAGATTTCCA TGAATTCTGC ATGAGAAAAC TGTGACTGAT ATGTCAGTTT TTTCACTTAG
 TTTATAGTAC ACGCAAAAAT
 R
 ACATGGCCAG TCTCTTGCCA TGTTATTTCC AAAGAAAATT ACTTGGAAAA TATACCTTTC
 ACCAAACTCT AAATCCATGT GCAAAATGTA ATATTTTATA CACCATATAA AAATACCAAA
 AAACATCTAG CAGTACCAAA TCAAGATGAG ACACAAGAGA GGGATCCTAT GCACTGGTAG
 CTGCAGGATG GCTTCTGTAG TAAGTTGTAT GGTGTGGTCT CCAATAAGAT ATgtcctaat
 cccagaacct aggaaggtga ccttattgga aaaaagggtc tctatagatg taagttaagg
 atttggggct gaagagatca ttccagatta tccagatggg ccctatgtcc aatgataaat
 gtccttataa gagggaggca gaggaagatt ggtccgagac aaaagagggg aacgtgatgt
 gaagagggag ggaaagatta gagagatatg accacacgtc caggaatgcc agggcatcac
 cagaagctgg gagagacaag gaacacattc tcccctggct ctccctcagg gcgtgtgacc
 ctgccagatt ttggagttcc agccttcaaa actgtgagta aaactatttc tattgctaaa
 gtcaccaagt gtgtggtgat ttaggatggc agccacagga aCAGTTTGAC TCCCTTCACC
 CGGAGTACAA TCCACGCACC TGCCAATCAA AGCAACAAAG TATGAAAATC ACTACTTTAA
 AAACTCAAGA CAAAAGAAAC C

  GeneView back to top
GeneView: no link established by analysis of contig annotation
GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs785448 maps exactly once on NCBI human chromosome 15
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
15NW_925796.110101087787574plusGalt_assembly_1CeleraCeleraview200
15NW_001838199.19462707811545plusGalt_assembly_8HuRefHuRefview200
15NT_010194.1693682027933555plusAref_assemblyreferencereferenceview200

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_010194 AC069382 AC069382.2
dbSNP Blast Analysis

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss1771810HapMap-CEUEuropean 106IG 0.019 0.132 0.849 0.150 0.085 0.915
HapMap-HCBAsian 70IG 0.057 0.943 0.029 0.971
HapMap-JPTAsian 78IG 1.000 1.000
HapMap-YRISub-Saharan African 114IG 0.018 0.982 0.009 0.991
ss66219492HapMap-CEUEuropean 118GF 0.102 0.898 0.051 0.949
HapMap-HCBAsian 90GF 1.000 1.000
HapMap-JPTAsian 90GF 1.000 1.000
HapMap-YRISub-Saharan African 120GF 1.000 1.000
ss69171732HapMap-CEUEuropean 120GF 1.000 1.000
HapMap-HCBAsian 90GF 1.000 1.000
HapMap-JPTAsian 90GF 1.000 1.000
HapMap-YRISub-Saharan African 120GF 1.000 1.000
Concordant GenotypeTotal SampleA/AA/GG/G
ss17718102604229
ss66219492259259
ss69171732260260
RefSNP Genotype SummaryTotal IndividualA/AA/GG/G
rs7854482704260
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss)GenotypePopulation
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
169ss1771810A/GCSHL-HAPMAPHapMap-CEUNA06994CEPH1340.09r23_ch15_CEU_affymetrix:genotype_protocol_15212696
169ss66219492G/GCSHL-HAPMAPHapMap-CEUNA06994CEPH1340.09chr15-HapMap-CEU
169ss69171732G/GCSHL-HAPMAPHapMap-CEUNA06994CEPH1340.09chr15-HapMap-CEU
215ss1771810A/GCSHL-HAPMAPHapMap-CEUNA10857CEPH1346.01r23_ch15_CEU_affymetrix:genotype_protocol_15212696
215ss66219492A/ACSHL-HAPMAPHapMap-CEUNA10857CEPH1346.01chr15-HapMap-CEU
215ss69171732G/GCSHL-HAPMAPHapMap-CEUNA10857CEPH1346.01chr15-HapMap-CEU
226ss1771810A/GCSHL-HAPMAPHapMap-CEUNA12044CEPH1346.12r23_ch15_CEU_affymetrix:genotype_protocol_15212696
226ss66219492A/GCSHL-HAPMAPHapMap-CEUNA12044CEPH1346.12chr15-HapMap-CEU
226ss69171732G/GCSHL-HAPMAPHapMap-CEUNA12044CEPH1346.12chr15-HapMap-CEU
361ss1771810A/GCSHL-HAPMAPHapMap-CEUNA11993CEPH1362.14r23_ch15_CEU_affymetrix:genotype_protocol_15212696
361ss66219492A/GCSHL-HAPMAPHapMap-CEUNA11993CEPH1362.14chr15-HapMap-CEU
361ss69171732G/GCSHL-HAPMAPHapMap-CEUNA11993CEPH1362.14chr15-HapMap-CEU
400ss1771810A/GCSHL-HAPMAPHapMap-CEUNA10831CEPH1408.02r23_ch15_CEU_affymetrix:genotype_protocol_15212696
400ss66219492A/GCSHL-HAPMAPHapMap-CEUNA10831CEPH1408.02chr15-HapMap-CEU
400ss69171732G/GCSHL-HAPMAPHapMap-CEUNA10831CEPH1408.02chr15-HapMap-CEU
410ss1771810A/ACSHL-HAPMAPHapMap-CEUNA12155CEPH1408.12r23_ch15_CEU_affymetrix:genotype_protocol_15212696
410ss66219492A/GCSHL-HAPMAPHapMap-CEUNA12155CEPH1408.12chr15-HapMap-CEU
410ss69171732G/GCSHL-HAPMAPHapMap-CEUNA12155CEPH1408.12chr15-HapMap-CEU
411ss1771810A/GCSHL-HAPMAPHapMap-CEUNA12156CEPH1408.13r23_ch15_CEU_affymetrix:genotype_protocol_15212696
411ss66219492A/GCSHL-HAPMAPHapMap-CEUNA12156CEPH1408.13chr15-HapMap-CEU
411ss69171732G/GCSHL-HAPMAPHapMap-CEUNA12156CEPH1408.13chr15-HapMap-CEU
548ss1771810A/GCSHL-HAPMAPHapMap-CEUNA12763CEPH1447.12r23_ch15_CEU_affymetrix:genotype_protocol_15212696
548ss66219492A/GCSHL-HAPMAPHapMap-CEUNA12763CEPH1447.12chr15-HapMap-CEU
548ss69171732G/GCSHL-HAPMAPHapMap-CEUNA12763CEPH1447.12chr15-HapMap-CEU
623ss1771810A/GCSHL-HAPMAPHapMap-CEUNA12878CEPH1463.02r23_ch15_CEU_affymetrix:genotype_protocol_15212696
623ss66219492A/GCSHL-HAPMAPHapMap-CEUNA12878CEPH1463.02chr15-HapMap-CEU
623ss69171732G/GCSHL-HAPMAPHapMap-CEUNA12878CEPH1463.02chr15-HapMap-CEU
636ss1771810A/GCSHL-HAPMAPHapMap-CEUNA12891CEPH1463.15r23_ch15_CEU_affymetrix:genotype_protocol_15212696
636ss66219492A/GCSHL-HAPMAPHapMap-CEUNA12891CEPH1463.15chr15-HapMap-CEU
636ss69171732G/GCSHL-HAPMAPHapMap-CEUNA12891CEPH1463.15chr15-HapMap-CEU
Genotype data submitted for270 samples from270 individualsIndividual with multiple genotypes submission:270

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwithHapMapFreqUNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .