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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs606629          
refSNP ID: rs606629
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:83/129
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
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 ss778710 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs606629 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
ss778710SC_JCM|AL355998.3_52462fwd/BC/Tacagccagggcaagtaaccttttcttgtcctcagtcctgcttatctcagcgccctgaatg07/27/0010/10/0383Genomicunknown
ss1075829KWOK|OVLP-000804-37931fwd/BC/Tacagccagggcaagtaaccttttcttgtcctcagtcctgcttatctcagcgccctgaatg09/02/0010/10/0386Genomic99 %
ss1714901KWOK|OVLP-000925-695776fwd/BC/Tacagccagggcaagtaaccttttcttgtcctcagtcctgcttatctcagcgccctgaatg10/05/0010/10/0387Genomic99 %
ss1715466KWOK|OVLP-000925-703613fwd/BC/Tacagccagggcaagtaaccttttcttgtcctcagtcctgcttatctcagcgccctgaatg10/05/0010/10/0387Genomic99 %
ss13025763SC_SNP|NT_021937.15_2734059rev/TA/Gcattcagggcgctgagataagcaggactgaggacaagaaaaggttacttgccctggctgt10/22/0310/31/03123Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs606629|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=123
 TCTTTCCACC ATGGGGAGGT CTCCATGCAA TATTCTTTTT GGAGTGAGCT TTCAGAGCCA
 GCCACAAAGC CAACTCCTTC TGACCTGGCC TCAGGGTCCC AGTGGGAATC TATCTTACAG
 GGTTGCTTGG ACAGCGGGAA CCCTACTCCT TCCCTGCTTA AGGCTGGCCC ACAGCCAGGG
 CAAGTAACCT TTTCTTGTCC
 Y
 TCAGTCCTGC TTATCTCAGC GCCCTGAATG TGCCGGGCCA GCCCCTTGAT GACTCATGTC
 CTAAAATCAC GAACAGGAAG CAGCATTTGG TGTTAGCCAC AGCTCTACAA CTGCCTGCTT
 CATCTGGCCC TCCTACCGGT CCTCCTCCCT TCCCTGGGGC CACATCTTGG GCTGAGCTGG
 CCATACCATG CTGTGGGCTG

  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:  rs606629 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_923572.1890474311335417minusGalt_assembly_1CeleraCeleraview200
1NW_001838534.1119270811375374minusGalt_assembly_8HuRefHuRefview200
1NT_021937.18675949212144712minusGref_assemblyreferencereferenceview200

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_021937 AC023251 AL355998.3 AL355998.4 AL357835.3
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AL357835.11 AL355998.9 BX510650.2

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/T
HWPC
T
ss778710SC_12_AAsian 24IG 1.000 1.000
SC_12_AAAfrican American 20IG 0.900 0.100 1.000 0.950 0.050
SC_12_CEuropean 12IG 1.000 1.000
SC_95_CEuropean 92IG 1.000 1.000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.013+/-0.0811257160

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

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Revised: May 25, 2006 1:38 PM .