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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs595725          
refSNP ID: rs595725
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:83/129
Map to Genome Build:36.3
Citation: PubMed
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:G/T
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
NM_000911.3:c.228-12751C>A
NT_004610.18:g.11997057C>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 ss1644280 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs595725 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
ss767587SC_JCM|AC023527.2_10035rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct07/27/0010/10/0383Genomicunknown
ss994056KWOK|OVLP-000804-22002fwd/BG/Tagagttagccatgtgaagtgaaggaggaagttggtccaaagagaaggaacagcatgtaca09/02/0010/10/0386Genomic97 %
ss1644280KWOK|OVLP-000925-493525byFreqfwd/BG/Tagagttagccatgtgaagtgaaggaggaagttggtccaaagagaaggaacagcatgtaca10/04/0010/25/0687Genomic97 %
ss2177394TSC-CSHL|TSC0550596byFreqrev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct10/19/0004/07/0488Genomic95 %
ss5544936TSC-CSHL|TSC0612717rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct09/21/0210/10/03108Genomicunknown
ss5680274SC_JCM|NT_004538.12_373495rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct01/10/0310/10/03111Genomicunknown
ss6405735WI_SSAHASNP|NT_004538.13_574198rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct02/12/0310/10/03111Genomicunknown
ss13003703SC_SNP|NT_004538.14_365671rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct10/22/0310/31/03119Genomicunknown
ss16385089CSHL-HAPMAP|CSHL-HuAA-200402.chr1.NT_004538.15_362021rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct02/17/0403/04/04120Genomicunknown
ss20438279SSAHASNP|WGSA-200403-chr1.chr1.NT_004538.15_362021rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct03/18/0403/18/04121Genomicunknown
ss24237359PERLEGEN|afd4507636byFreqrev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct08/10/0409/13/04123Genomicunknown
ss44047021ABI|hCV2962139rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct07/18/0507/18/05126Genomicunknown
ss65920000AFFY|SNP_A-1748629rev/TA/Catgctgttccttctctttggaccaacttcctccttcacttcacatggcta10/26/0610/26/06127Genomicunknown
ss78297937HGSV|Cor12878_SNV_20070510.chr1_28993331rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct10/17/0710/18/07129Genomicunknown
ss82990987HGSV|Cor18956_SNV_20070510.chr1_28993331rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct11/30/0712/04/07130Genomicunknown
ss87323529BCMHGSC_JDW|JWB-0027909rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct02/26/0802/26/08129Genomicunknown
ss1080838851000GENOMES|CEU.trio.12.15.2008_36456_chr1_29045302rev/TA/Ctgtacatgctgttccttctctttggaccaacttcctccttcacttcacatggctaactct12/15/0812/15/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs595725|allelePos=1272|totalLen=4495|taxid=9606|snpclass=1|alleles='G/T'|mol=Genomic|build=130
 CATGTACAAC GTCAAAGAAC CTGGGCCCTT CCATTTAAGT GCACTCATGT CAATTTGGGC
 TGGACCTCTG CCCTGGTCCT GTCACCTCTG AGGTGTCCTC AGGTCAGAAA TGCAAACAGG
 CTCggctggg cgcggtagct cacggctgta atcccagcac tttgggaggc caaggcaggc
 agatcacctg aagtcaggag tttaagacca gcctggccaa catggcgaaa ccccatctct
 attaaaaaca taaaaattag ctgggcatgg tggcgggcac ctgtaatccc agctactcag
 gaggctgaag taggagaatt ggttgaaccc gggaggcaga ggttgcagtg agctgagatc
 gcgccactga actccagcct gggccacaag agccaaactc cgtcggaaag gaaaggggac
 aggaaagggg aaaggaaagg ggacaggaaa ggggacagga aaggaaagga agggaaagga
 agaaagtaaa gaaaggaagg aaggaagaaa gagagaaaga gaaagaaaag gaaggaagga
 aggaagaaaa agaaagaaag aaagaaaaag aaagaaagag aaaagaaaga aagaaagaaa
 gaaagaaaga aagaaagaaa gaaagaaaag aaagaaagaa agaaagaaag aaaATGCAAA
 CAGCCTCCAT GTGATACAAC TCTGAATAAA TACAATGGGG CCTTTGGGAT GGTGGGATTA
 CTGCACTTAC AAGAGAGGCC CCAGAGAGCT TGCTCGCTCT CTCTCTCTCt tttttttttt
 ttttcttttt ttgagacaga gtcttgctct gtcgcccagg ctggagtgca gtgctgtaat
 ctcggctcac tgcaacctcc acctcctggg ttcaagcgat tctcgtgcct cagcctccct
 agtagctggg attacaggcg cccaccacca cgcccagcta atttttgtat ttttagtaga
 gatgcggttt cactatgttg gccaggctgg tctccagctc ctgacctcag gtgatctgcc
 cgAGTTTGCT CTCTctctct ttctctctgc catgtgaggg cagtgatgag gcagccatct
 agaggccagg aagacagccc tcaccagaac ctgaccgtgg tggcagcttg atcttgggct
 tctgtcctta cgaactgaga aactaaatct ctgttgttga agccatccag tctatatttt
 gATCTAAGAC ACAGCAACAT TTCTGCCAGG TTGgaaggat gagagttagc catgtgaagt
 gaaggaggaa g
 K
 ttggtccaaa gagaaggaac agcatgtaca aagtccctgt agcaggaaag agcctgatgg
 gctgcaggaa tggtcagaaa tcacatgtga cgacagtgta gtgagccaga aaggaggcaa
 caggagaggc ggcagcggaa atctgcagga gtcaaatcac acagggcctt tgggctatgg
 caagaagttt gggtttactc tgagtgtaac aggaagccat tgaagacttt aaacagggaa
 gtgatgtggt tcatttatgt gagtttctta aaagatcacg ctgactactg tgtggaagcc
 agatggagca caaggcagta gggagccagA GACCCAACTT TCTAGAAAGA GAAATTGTTT
 ATGGCTCCAT TTCCCAAAAC TCTACTGTTG TTCTCTAATT TTTTTTTCTG TTACAAAAGG
 TTGTGGATat gaagttgggc ctttccctta caccatatac aaaaattaac tcaaaatgga
 tcaaagatgt aagagctaaa accataaaac tcctagaaga aaatatagtg ggaaagcttc
 atgacaccag atttggcaat gatttcttGT GTTTATTTGT TTGTTTTTCT TTCTTTTTTT
 CCTCTTTTTT AAATTTCTTc ttagatttgg caatgatttc ttggatatga caccaaaagc
 ctaggccaca acaacaacaa caactacatt aagttggact atatcaattt tttttttttt
 ttttgagatg gagtctcact ctgtcgccca ggctggagtg cagtggtgca atctcggctc
 actgcaacct ctgcctcata attctcccgc ctcagcctcc caagcacctg ggattatagg
 ctcccaccag catgcccggc taattttttt tttgtatttt tagtagagac agggtttcac
 tatgtttacc aggctagtct tgaactcctg acctcaagtt atccacctac ctcggcctcc
 caaagagctg ggattacagg catgagccac cgtgcctggc cccagctaat ttttgtattt
 ttagtagaga cggggtttca ccatattggt aaggctggtc tcgaactcct gaccttgtga
 tctgcccgcc ttggcctccg aaagtgctgg gattacaggc atgagccacc atgcccggct
 gactatatca catttaaaac ttttgtgcct caaatgacac tatcatccca ggactttggg
 aggccaaggc aggtgggtca cctgaggtca ggagtttgag accagtctct ccaacatgct
 gaaaccccat ctctacaaaa aaatacaaaa attagccgag agtggtagtg cacacctgta
 atcccagcta ctcgggagac tgaggcacaa gaatcgcttg aacctgggag gtggaggttg
 cagtgagccg agattgtgcc actgcactcc agtctgggta acacagtgag actctgtcac
 cccctcaaaa aaacaaaaac aaatgacact gtcaacagaa tgaaaaggtc actcatggaa
 tgggagaaaa gatttgcaaa tcacatatct gataaggggt taatatccag actatataaa
 gaattcctac aactcaacca aaagcaaata agttaattaa aaaatgaaca agggctgagc
 acagtagctc acatctgtaa tcctagcact ttgggaggct gaggtgggtg gatcgcttga
 gtccaagagt ttgagaccag cctggccaac atggcaaaac cccatctcta caaaaaatac
 aaaaattagc tgggcatggt gacatgcgct tgtagtccca gctacttgga gggccgaggt
 gggagaatcg cttgagtcct ggaggtcgag gctgcagtga gccatgatta caccactaca
 ctccagcctg aacgacaaag tgagaccctg tcttgaatat ttccctaaaa aagatataca
 aatggccaat aagcccatga aaagatgctc aacatcacta tcattaggga aatgcaaatc
 aaaaccacaa tgagatacca cttcacacct attaagataa tgaaaaaaaa aaaaaaaaca
 gaaatcaagt attggcaagg atttgaagaa actggaactc tcgtgtaccg tttttggaaa
 tgtaaaatgg tgcagccact gtggaaaaca aaactgtaat tcctcacaaa tctgaaaata
 gaattgcctc ttatgatcaa tccaacagtt cctcttctgg tagaagaatt aaaagcaggg
 ttttgaagag ctgtgtgtat acccatgttc atagcagtat tcttcataat agctaaaagg
 tgaaagcaac ccatatatcc attgatagat ggagaaacaa aatgtggtat agacatacaa
 tggaatatta ttcaccctta aaaaagaagg aaatTTCTAG CCTGGTGGCA AAGCCAGTTT
 TACAAAAAAT ACAAAAATTA gccgggcgtg gtgatgcacg tttgtagtcc cagctactcg
 ggaggctgag gtggaatgac tgcttgaccc cgaagttgag gttgcagtaa gccgagatca
 caccactgca ctccagcatg ggcgacagag caagagcctg tctcaaaaga caaaaaaaaG
 aagaagaagg aaattctgac acctgctaca acaaggatga accttgagga tatcgtgcta
 aataaaattt gccagtcaaa aaagacaaac actgaatgat tccacttaca tgaggcacct
 agagtagtca cagtcataga ggcagaagcc ctggggttac gaggggctag ggcaagggga
 ggatgggcag ttactgctta aatggtatgg agattcagtt tgggaagatg aaaaacttct
 ggagacgaac ggttgtgatg gctgcataac agtgtgaatg tacttaatgc cactgaacta
 cacccttaaa aatggttaca atggtatttt ttatgttgtg tatattttat cacaataaaa
 aaGGCGGTAA TCAAGAGCTG TCGCTGTGTT TATTTTCTAA GCTTGGGAGT GGGGTGAGGG
 GGTCCTTTCG AGCCATTCAG ATCTTGGCTC CCCAACATAC ATAGCTCAGT GATCTTGAGC
 AAGTCACTTC ACCTTTCTGA ACCTGCTTCC TTGTTGGTAA TTTCAGTGTA ATGATGCTTT
 CTAGGAGCCG CACGTGTGAA AGCGTGCAGC ATACAAGCCA GTGTGTAGTT GAAAATTGCA
 GCCCTTTTGG TACTCCCTGA CCTGGTATTT TTCTTTTTCT TCT

  GeneView back to top
GeneView via analysis of contig annotation: OPRD1 opioid receptor, delta 1
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_004610->NM_000911
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_004610->NM_000911->NP_00090211997057forwardintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs595725 maps exactly once on NCBI human chromosome 1
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
1NW_001838576.1306995127425129minusCalt_assembly_8HuRefHuRefview1271
1NW_921351.1342971627568858minusAalt_assembly_1CeleraCeleraview1271
1NT_004610.181199705729045302minusCref_assemblyreferencereferenceview1271

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_004538.12 AL009181 AL356786 AL356786.4 AL356786.5
dbSNP Blast Analysis
GenBank HTGS Finished:
AL009181.1

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceG/G
G/T
T/T
HWPG
T
ss1644280HapMap-CEUEuropean 120IG 0.300 0.467 0.233 0.655 0.533 0.467
HapMap-HCBAsian 90IG 0.022 0.244 0.733 1.000 0.144 0.856
HapMap-JPTAsian 88IG 0.023 0.205 0.773 0.752 0.125 0.875
HapMap-YRISub-Saharan African 120IG 0.700 0.300 0.200 0.850 0.150
CHMJAsian 74IG 0.162 0.838
ss2177394AfAmAfrican American 40IG 0.650 0.250 0.100 0.251 0.775 0.225
CaucasianEuropean 40IG 0.200 0.500 0.300 1.000 0.450 0.550
AsianAsian 40IG 0.050 0.200 0.750 0.343 0.150 0.850
CEPHEuropean 56IG 0.357 0.500 0.143 1.000 0.607 0.393
PDpanelGlobal 48IG 0.333 0.333 0.333 0.150 0.500 0.500
ss24237359AFD_EUR_PANELEuropean 48IG 0.167 0.542 0.292 0.655 0.438 0.562
AFD_AFR_PANELAfrican American 46IG 0.565 0.261 0.174 0.100 0.696 0.304
AFD_CHN_PANELAsian 48IG 0.125 0.875 0.752 0.062 0.938

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
Additional Freq. Data
0.496+/-0.042429355340ALFRED: The Allele Frequency Database

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqwith2hitwithHapMapFreq
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .