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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs149156          
refSNP ID: rs149156
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:79/129
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
NT_010498.15:g.20526905T>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 ss1714814 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs149156 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
ss224876KWOK|OVLP-000621-16513fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt06/30/0010/10/0379Genomic96 %
ss230551KWOK|OVLP-000621-348889fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt06/30/0010/10/0379Genomic95 %
ss628802SC_JCM|AC027131.2_142745fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt07/12/0010/10/0380Genomicunknown
ss956249KWOK|OVLP-000804-432860rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga09/01/0010/10/0386Genomic99 %
ss1033690KWOK|OVLP-000804-441043rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga09/02/0010/10/0386Genomic97 %
ss1068475KWOK|OVLP-000804-424453fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt09/02/0010/10/0386Genomic81 %
ss1714814KWOK|OVLP-000925-694571byFreqrev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga10/05/0004/07/0492Genomic99 %
ss1744754KWOK|OVLP-000925-690480rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga10/05/0010/10/0392Genomic97 %
ss1756850KWOK|OVLP-000925-685126fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt10/05/0010/10/0392Genomic81 %
ss14263443BCM_SSAHASNP|chr16.NT_010498.14_15634259rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga11/05/0311/22/03119Genomicunknown
ss17562723CSHL-HAPMAP|CSHL-HuCC-200402.chr16.NT_010498.14_15634259rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga02/19/0403/04/04120Genomicunknown
ss43948788ABI|hCV2287344rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga07/18/0507/18/05126Genomicunknown
ss65715874ILLUMINA|Human1-rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt10/10/0610/10/06127Genomicunknown
ss67117098ILLUMINA|HumanHap550v1.1_rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt11/14/0611/14/06127Genomicunknown
ss67454754ILLUMINA|HumanHap650Yv1.0_rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt11/14/0611/14/06127Genomicunknown
ss68156793ILLUMINA|HumanHap250Sv1.0_rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt12/06/0612/07/06127Genomicunknown
ss70624434ILLUMINA|HumanHap550v3.0__rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt04/20/0703/30/08130Genomicunknown
ss71173558ILLUMINA|HumanHap650Yv3.0_rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt04/23/0704/23/07127Genomicunknown
ss74830409AFFY|SNP_M-587186fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt08/09/0708/09/07128Genomicunknown
ss75881341ILLUMINA|ILMN_Human_1M_rs149156fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt08/28/0708/29/07129Genomicunknown
ss78203722HGSV|Cor12878_SNV_20070510.chr16_65470207rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga10/17/0710/18/07129Genomicunknown
ss82299030HGSV|Cor18555_SNV_20070510.chr16_65470207rev/BC/Taaaataatttataaggaagcaggtcatcacggaatgccacaatgttaggaccagaaggga11/27/0712/02/07130Genomicunknown
ss83367665KRIBB_YJKIM|KHS444895fwd/TA/Gtcccttctggtcctaacattgtggcattccgtgatgacctgcttccttataaattatttt12/04/0712/04/07130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs149156|allelePos=1079|totalLen=1279|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 TTGATTTTAC GGTTTTCCCT CCTCCACCTT TGACTTGGTC CTAACCACAG AGCAGAGCAG
 CCAGAATGAC GCCCCTCCCA CCTTTTCTCG TGGTTGGTGG gtagagacaa ggtctttcta
 tgttgcccag gctggtctca aactgccagg ctcaagcaat cctcccacct cagcctcccc
 aaagtgctgg gattacagac gtgagccatc acgcctggcA GAATGACACT TCTAAAACTC
 AAATTCCAAg gccgagtgcg gtggctcctg cctgtaatcc cagcactttg ggaggccgag
 gcggggggat ctcctgaggt caggagtttg agaccagcct ggccaacatc acgaaaccgt
 ctctactaaa aatacaaaaa ttagctggga gtggtggtgc gcgcctgtag tcccagctac
 ctgggaggct gaggcatgag aatcatttga accagggagg tggaagttgc actgaggtga
 gatcatgcca ctgcacgcca gcctgggaga cagagtgaga gtctgtctca aaaaaaacaa
 aaacagaaac aaaaacaaaC CAAAAAAACC CTCAAATTCC TGCCCTAAAG TCtttttttt
 tttttttttt ttttttttga gacggagtct cgctctgtcg cccaggctgg agtgcagtgg
 cgggatctcg gctcactgca agctccgcct cccgggttca cgccattccc ctgcctcagc
 ctcccaagta gctgggacta caggcgcccg ccactacgcc cggctaattt tttgtatttt
 tagtagagac ggggtttcac cgttttagcc gggatggtct cgatctcctg acctcgtgat
 ccgcccgcct ccgcctccca aagtgctggg attacaggca tgagccaccg cgcccggccT
 CCTGCCCTAA AGTCTTTAGT GGTTTCCCAC AAACCATTAA GCTTTGAACT GACCATTATA
 TTGGCCTGCT ACTGACAATT AACTCAGCAC GGCTGGCGGC TGGTAGGTTG AGAGAGACAG
 CGAACCCCGA CACCAGATAA TCCCTCCGTC CCTTCTGGTC CTAACATTGT GGCATTCC
 R
 GTGATGACCT GCTTCCTTAT AAATTATTTT CACAGAACTC TTGTAACTAT GGTAAGTCAG
 ATGGAGTCCT TCCCTGGAGA CAGAGAAAAA TGGGAGACAA CCAGAAAAAG CCACTTGGAG
 CCCTGAGAGT GTGGTTTTCC AGAAGGAAGA CACACTGGCT TACCTGGGCA GCCTGGCCAG
 CCTCCTGGAC CCAAGGACGT

  GeneView back to top
GeneView via analysis of contig annotation: PDP2 pyruvate dehydrogenase phosphatase isoenzyme 2
View variations for gene:
Include clinically associated: in gene region cSNP has frequency double hit
Group
Label
Contig->mRNAGene Model (contig mRNA transcript) Color Legend
referenceNT_010498->NM_020786
svfunction
CeleraNW_926462->NM_020786
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_010498->NM_020786->NP_06583720526905forward5' near gene
CeleraNW_926462->NM_020786->NP_06583720485802forward5' near gene

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs149156 maps exactly once on NCBI human chromosome 16
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
16NW_926462.12048580251421003minusTalt_assembly_1CeleraCeleraview1078
16NT_010498.152052690565470207minusTref_assemblyreferencereferenceview1078

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_010498 AC004638 AC026399 AC027131.3 AC044802.2
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AC004638.1 AC026397.4 AC027131.6 AC044802.6 NC_000016.8 AC026399.4

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceA/A
A/G
G/G
HWPA
G
ss1714814CEPH 184AF 0.390 0.610
HapMap-CEUEuropean 120IG 0.233 0.417 0.350 0.251 0.442 0.558
HapMap-HCBAsian 90IG 0.111 0.444 0.444 1.000 0.333 0.667
HapMap-JPTAsian 88IG 0.159 0.523 0.318 0.655 0.420 0.580
HapMap-YRISub-Saharan African 120IG 0.017 0.133 0.850 0.343 0.083 0.917

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.429+/-0.17527021000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqbySubmitterwithHapMapFreq
Validated by: ILLUMINA
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .