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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs155256          
refSNP ID: rs155256
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:C/T
Ancestral Allele:C
Clinical Association:unknown
HGVS Names
NT_037887.4:g.2242565G>A
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 ss1617454 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs155256 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
ss292874KWOK|OVLP-000621-280596rev/TA/Gctgtaatcccagcactttgggggccaaggtggcaaatcatgaggtcaggagtttgagacc06/30/0010/10/0379Genomic97 %
ss342993KWOK|OVLP-000621-94470rev/TA/Gctgtaatcccagcactttgggggccaaggtggcaaatcatgaggtcaggagtttgagacc06/30/0010/10/0379Genomic99 %
ss402704KWOK|OVLP-000621-250530rev/TA/Gctgtaatcccagcactttgggggccaaggtggcaaatcatgaggtcaggagtttgagacc06/30/0010/10/0385Genomic99 %
ss413204KWOK|OVLP-000621-277658rev/TA/Gctgtaatcccagcactttgggggccaaggtggcaaatcatgaggtcaggagtttgagacc06/30/0010/10/0385Genomic99 %
ss1144033KWOK|OVLP-000804-425428fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag09/02/0010/10/0386Genomic99 %
ss1145416KWOK|OVLP-000804-433218fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag09/02/0010/10/0386Genomic99 %
ss1238663KWOK|OVLP-000804-417835fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag09/02/0010/10/0386Genomic97 %
ss1238970KWOK|OVLP-000804-420779fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag09/02/0010/10/0386Genomic97 %
ss1617454KWOK|OVLP-000925-522660fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag10/04/0010/10/0387Genomic99 %
ss1645448KWOK|OVLP-000925-513719fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag10/04/0010/10/0392Genomic97 %
ss1646013KWOK|OVLP-000925-524957fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag10/04/0010/10/0387Genomic97 %
ss2480561SC_JCM|AC012171.4_236536fwd/BC/Tggtctcaaactcctgacctcatgatttgccaccttggcccccaaagtgctgggattacag11/03/0010/10/0389Genomicunknown
ss14260194BCM_SSAHASNP|chr16.NT_037887.3_2242488rev/TA/Gctgtaatcccagcactttgggggccaaggtggcaaatcatgaggtcaggagtttgagacc11/05/0311/22/03119Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs155256|allelePos=562|totalLen=887|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=119
 GCAAATCTAG TTCTGGGTTC ACTGCCTTCT CACTTGTCCC CTCGCCCCTA GTAACTTTCT
 GTTCCTCACC ATCCGCAGTG GCACCTCCGA TGCTTTCAGC CAGGAGAACC TAGGGTTTGT
 GTGCTGTGGG GACCAGGTTG CTCCTAGGGT GGACAAATAG AAGGAGATGG TTTTATCGCC
 ACCTTGGAAT GTGTGTGTGt tttcagacag actctcgctc tgtcacccag gctggagtat
 gtaccatggt gcgatcatag ctcattacag cctccaactc ctTCTTCAGT GTCCAGAGTA
 GCAGGGGCTA Attttttttt aattttttaa tttttttttt gagacagtct ctgttgcctg
 ggttggagtg cagtggcgca atattggctc actacaacct ctgcctcctg ggttcaagtg
 attttcctgc ctcagcctcc tgagtagctg gaattacagg cacctgccac catgcccagc
 taattttttg tatttctagt agagacgggg tttcatcata ttggcccggc tggtctcaaa
 ctcctgacct catgatttgc c
 Y
 accttggccc ccaaagtgct gggattacag gcgtgagcca ccgcgcccag cAGCAGGAGC
 TAATTTTTAA GAATTTTTTG TAGCAACAAG TTGTTGCTAT GTTACCCAGC TGGTCCTGAG
 TCACTGGGGT TACAGGTGTG TGTCACCATG CCAGGCTTGC TTCCTCCTCC GTTAAGTGGC
 CATTTTTCCA CCTCAAAAAT TGGTTTGGGA CACAAGGAAG AATTGGAAAT GCTTAAGATG
 AGAACAAAAG TTGAGACCAC CCAACACAGC TGGGACCTTA CTGCCCAGTG CTCCCAGTGG
 TCTGACCAAA ACCCCACACC AGACA

  GeneView back to top
GeneView via analysis of contig annotation: DCI dodecenoyl-Coenzyme A delta isomerase (3,2 trans-enoyl-Coenzyme A isomerase)
View variations for gene:
Include clinically associated: in gene region cSNP has frequency double hit
GeneView via analysis of contig annotation: RNPS1 RNA binding protein S1, serine-rich domain
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
HuRefNW_001838339->NM_001919
svfunction
referenceNT_037887->NM_006711
svfunction
referenceNT_037887->NM_080594
svfunction
CeleraNW_926018->NM_006711
svfunction
CeleraNW_926018->NM_080594
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
HuRefNW_001838339->NM_001919->NP_001910395407forward5' near gene
referenceNT_037887->NM_006711->NP_0067022242565reverse3' near gene
referenceNT_037887->NM_080594->NP_5421612242565reverse3' near gene
CeleraNW_926018->NM_006711->NP_0067022232642reverse3' near gene
CeleraNW_926018->NM_080594->NP_5421612232642reverse3' near gene

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs155256 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_001838339.23954072228610plusCalt_assembly_8HuRefHuRefview561
16NT_037887.422425652242565minusGref_assemblyreferencereferenceview561
16NW_926018.122326422516992minusGalt_assembly_1CeleraCeleraview561

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_037887 AC024088 AC024088.4
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AC005212.1 AC007162.1 AC009065.8 AC098805.2 NC_000016.8 AC012171.4

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
HWPC
ss1617454HapMap-CEUEuropean 120IG 1.000 1.000
HapMap-HCBAsian 90IG 1.000 1.000
HapMap-JPTAsian 90IG 1.000 1.000
HapMap-YRISub-Saharan African 118IG 1.000 1.000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
27021000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterwith2hitwithHapMapFreq
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .