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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs16902944          
refSNP ID: rs16902944
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:123/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/G
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
NM_145000.2:c.91+376C>G
NT_006576.15:g.36273809G>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 ss85257779 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs16902944 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
ss23415578PERLEGEN|afd3106928byFreqfwd/TC/Gacaaacttaggcttaaacaaagtgaaaaaatgtcccaccagtggtactatggtagagaaa08/10/0409/13/04123Genomicunknown
ss66116422AFFY|SNP_A-2026493byFreqfwd/TC/Gaaacaaagtgaaaaaatgtcccaccagtggta10/27/0603/31/08127Genomicunknown
ss76103616AFFY|AFFY_6_1M_SNP_A-2026493fwd/C/Gaaacaaagtgaaaaaatgtcccaccagtggta08/28/0708/30/07129Genomicunknown
ss85257779HGSV|Cor18517_SNV_20070510.chr5_36336809fwd/C/Gacaaacttaggcttaaacaaagtgaaaaaatgtcccaccagtggtactatggtagagaaa12/06/0712/08/07130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs16902944|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/G'|mol=Genomic|build=130
 AAAGACTGAT GGTGAAAATG GCTGGGAGGT AGATAGTTTA GTTTGAATGA GTGCCCAGCA
 AGTGAAATGT GACACTTTTC CCTGACTGTC TCCAGATGTC CCTGGACCAT AAAAAGGAAA
 GAGTCAAGAA TATATTTATT TTTCCCACAA TGAATGAGCC AGAGATCCAG ACAAACTTAG
 GCTTAAACAA AGTGAAAAAA
 S
 TGTCCCACCA GTGGTACTAT GGTAGAGAAA GCTCCAGGCT AACTTAAAGC TACTCTCAGC
 TGAAATCCCC CTTGTAGCTG ACTCAGCCTT GCTCAGATGG GTGTTTTGAA TTAGACAAAA
 TCTAGCATAC TCTAAAAAAC ACAGTGGCTA GAAGTTTAAG CATGTAAGTT TCAGAATGAC
 AGCTCCAAGG AATATGCATT

  GeneView back to top
GeneView via analysis of contig annotation: RANBP3L RAN binding protein 3-like
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_006576->NM_145000
svfunction
HuRefNW_001838933->NM_145000
svfunction
CeleraNW_922596->NM_145000
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_006576->NM_145000->NP_65943736273809reverseintron
HuRefNW_001838933->NM_145000->NP_659437595303reverseintron
CeleraNW_922596->NM_145000->NP_6594371897237reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs16902944 maps exactly once on NCBI human chromosome 5
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
5NW_922596.1189723736186723plusGalt_assembly_1CeleraCeleraview100
5NW_001838933.159530336252692plusGalt_assembly_8HuRefHuRefview100
5NT_006576.153627380936336809plusGref_assemblyreferencereferenceview100

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NC_000005.5
dbSNP Blast Analysis
GenBank HTGS Finished:
AC026439.4 AC114277.2 NC_000005.8

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/G
G/G
HWPC
G
ss23415578AFD_EUR_PANELEuropean 48IG 1.000 1.000
AFD_AFR_PANELAfrican American 46IG 0.087 0.435 0.478 1.000 0.304 0.696
AFD_CHN_PANELAsian 48IG 1.000 1.000
HapMap-CEUEuropean 114IG 1.000 1.000
HapMap-HCBAsian 88IG 1.000 1.000
HapMap-JPTAsian 80IG 1.000 1.000
HapMap-YRISub-Saharan African 118IG 0.153 0.492 0.356 0.527 0.398 0.602
ss66116422HapMap-CEUEuropean 118GF 1.000 1.000
HapMap-HCBAsian 90GF 1.000 1.000
HapMap-JPTAsian 90GF 1.000 1.000
HapMap-YRISub-Saharan African 120GF 0.033 0.417 0.550 0.242 0.758
Concordant GenotypeTotal SampleC/CC/GG/G
ss23415578307635255
ss66116422244228214
RefSNP Genotype SummaryTotal IndividualC/CC/GG/G
rs16902944332638265
Discordant Genotypes:
Indiviudal
SampleID
SubSNP(ss)GenotypePopulation
Handle
Submitter
Population
Submitter
SampleID
SampleID
Alias
Submission
Batch
NCBI
ProbeID
5134ss23415578C/GCSHL-HAPMAPHapMap-YRINA19127YOR077.02r23_ch5_YRI_affymetrix:genechip500k2851204
5134ss66116422G/GCSHL-HAPMAPHapMap-YRINA19127YOR077.02chr5-HapMap-YRI
5135ss23415578C/CCSHL-HAPMAPHapMap-YRINA19128YOR077.03r23_ch5_YRI_affymetrix:genechip500k2851204
5135ss66116422C/GCSHL-HAPMAPHapMap-YRINA19128YOR077.03chr5-HapMap-YRI
5136ss23415578C/GCSHL-HAPMAPHapMap-YRINA19132YOR101.01r23_ch5_YRI_affymetrix:genechip500k2851204
5136ss66116422G/GCSHL-HAPMAPHapMap-YRINA19132YOR101.01chr5-HapMap-YRI
5137ss23415578C/GCSHL-HAPMAPHapMap-YRINA19131YOR101.02r23_ch5_YRI_affymetrix:genechip500k2851204
5137ss66116422G/GCSHL-HAPMAPHapMap-YRINA19131YOR101.02chr5-HapMap-YRI
5139ss23415578C/GCSHL-HAPMAPHapMap-YRINA19100YOR105.01r23_ch5_YRI_affymetrix:genechip500k2851204
5139ss66116422G/GCSHL-HAPMAPHapMap-YRINA19100YOR105.01chr5-HapMap-YRI
5140ss23415578C/GCSHL-HAPMAPHapMap-YRINA19099YOR105.02r23_ch5_YRI_affymetrix:genechip500k2851204
5140ss66116422G/GCSHL-HAPMAPHapMap-YRINA19099YOR105.02chr5-HapMap-YRI
5141ss23415578C/CCSHL-HAPMAPHapMap-YRINA19098YOR105.03r23_ch5_YRI_affymetrix:genechip500k2851204
5141ss66116422C/GCSHL-HAPMAPHapMap-YRINA19098YOR105.03chr5-HapMap-YRI
5143ss23415578C/GCSHL-HAPMAPHapMap-YRINA19193YOR112.02r23_ch5_YRI_affymetrix:genechip500k2851204
5143ss66116422G/GCSHL-HAPMAPHapMap-YRINA19193YOR112.02chr5-HapMap-YRI
5238ss23415578C/CCSHL-HAPMAPHapMap-YRINA18503YOR005.01r23_ch5_YRI_affymetrix:genechip500k2851204
5238ss66116422C/GCSHL-HAPMAPHapMap-YRINA18503YOR005.01chr5-HapMap-YRI
5241ss23415578C/GCSHL-HAPMAPHapMap-YRINA18506YOR009.01r23_ch5_YRI_affymetrix:genechip500k2851204
5241ss66116422G/GCSHL-HAPMAPHapMap-YRINA18506YOR009.01chr5-HapMap-YRI
5245ss23415578C/GCSHL-HAPMAPHapMap-YRINA18858YOR012.02r23_ch5_YRI_affymetrix:genechip500k2851204
5245ss66116422G/GCSHL-HAPMAPHapMap-YRINA18858YOR012.02chr5-HapMap-YRI
5246ss23415578C/GCSHL-HAPMAPHapMap-YRINA18859YOR012.03r23_ch5_YRI_affymetrix:genechip500k2851204
5246ss66116422G/GCSHL-HAPMAPHapMap-YRINA18859YOR012.03chr5-HapMap-YRI
5250ss23415578C/CCSHL-HAPMAPHapMap-YRINA18521YOR016.01r23_ch5_YRI_affymetrix:genechip500k2851204
5250ss66116422G/GCSHL-HAPMAPHapMap-YRINA18521YOR016.01chr5-HapMap-YRI
5252ss23415578C/CCSHL-HAPMAPHapMap-YRINA18522YOR016.03r23_ch5_YRI_affymetrix:genechip500k2851204
5252ss66116422C/GCSHL-HAPMAPHapMap-YRINA18522YOR016.03chr5-HapMap-YRI
5255ss23415578C/GCSHL-HAPMAPHapMap-YRINA18871YOR017.03r23_ch5_YRI_affymetrix:genechip500k2851204
5255ss66116422G/GCSHL-HAPMAPHapMap-YRINA18871YOR017.03chr5-HapMap-YRI
5259ss23415578C/CCSHL-HAPMAPHapMap-YRINA18857YOR023.01r23_ch5_YRI_affymetrix:genechip500k2851204
5259ss66116422C/GCSHL-HAPMAPHapMap-YRINA18857YOR023.01chr5-HapMap-YRI
5260ss23415578C/CCSHL-HAPMAPHapMap-YRINA18855YOR023.02r23_ch5_YRI_affymetrix:genechip500k2851204
5260ss66116422C/GCSHL-HAPMAPHapMap-YRINA18855YOR023.02chr5-HapMap-YRI
5269ss23415578C/GCSHL-HAPMAPHapMap-YRINA19093YOR040.02r23_ch5_YRI_affymetrix:genechip500k2851204
5269ss66116422G/GCSHL-HAPMAPHapMap-YRINA19093YOR040.02chr5-HapMap-YRI
5275ss23415578C/CCSHL-HAPMAPHapMap-YRINA19137YOR043.02r23_ch5_YRI_affymetrix:genechip500k2851204
5275ss66116422C/GCSHL-HAPMAPHapMap-YRINA19137YOR043.02chr5-HapMap-YRI
5276ss23415578C/GCSHL-HAPMAPHapMap-YRINA19138YOR043.03r23_ch5_YRI_affymetrix:genechip500k2851204
5276ss66116422G/GCSHL-HAPMAPHapMap-YRINA19138YOR043.03chr5-HapMap-YRI
5285ss23415578C/GCSHL-HAPMAPHapMap-YRINA19203YOR048.03r23_ch5_YRI_affymetrix:genechip500k2851204
5285ss66116422G/GCSHL-HAPMAPHapMap-YRINA19203YOR048.03chr5-HapMap-YRI
5292ss23415578C/GCSHL-HAPMAPHapMap-YRINA19161YOR056.01r23_ch5_YRI_affymetrix:genechip500k2851204
5292ss66116422G/GCSHL-HAPMAPHapMap-YRINA19161YOR056.01chr5-HapMap-YRI
5297ss23415578C/CCSHL-HAPMAPHapMap-YRINA19223YOR058.03r23_ch5_YRI_affymetrix:genechip500k2851204
5297ss66116422C/GCSHL-HAPMAPHapMap-YRINA19223YOR058.03chr5-HapMap-YRI
5300ss23415578C/GCSHL-HAPMAPHapMap-YRINA19119YOR060.03r23_ch5_YRI_affymetrix:genechip500k2851204
5300ss66116422G/GCSHL-HAPMAPHapMap-YRINA19119YOR060.03chr5-HapMap-YRI
5302ss23415578C/GCSHL-HAPMAPHapMap-YRINA19140YOR071.02r23_ch5_YRI_affymetrix:genechip500k2851204
5302ss66116422G/GCSHL-HAPMAPHapMap-YRINA19140YOR071.02chr5-HapMap-YRI
Genotype data submitted for341 samples from332 individualsIndividual with multiple genotypes submission:269

  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 .