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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs10904559          
refSNP ID: rs10904559
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:120/129
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

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 ss39770866 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs10904559 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
ss15789896SC_SNP|NT_077567.3_73803fwd/BC/Tcaccaggacctgggggaagcacaggcacaaggccacagctgagagctgacccaggcccca11/17/0311/22/03120Genomicunknown
ss16481019CSHL-HAPMAP|CSHL-HuAA-200402.chr10.NT_077567.3_73803fwd/BC/Tcaccaggacctgggggaagcacaggcacaaggccacagctgagagctgacccaggcccca02/17/0403/04/04120Genomicunknown
ss18878936SC_SNP|SC-CHR9-12_NA07340-200402.chr10.NT_077567.3_73803fwd/BC/Tcaccaggacctgggggaagcacaggcacaaggccacagctgagagctgacccaggcccca02/20/0403/04/04120Genomicunknown
ss39770866ABI|hCV30931535fwd/BC/Tcaccaggacctgggggaagcacaggcacaaggccacagctgagagctgacccaggcccca07/16/0507/16/05126Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs10904559|allelePos=301|totalLen=601|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=126
 AGCAGGCACT ACTCTAACCC CACTCCACCC TACTCCTGGC AGCCTATCCA GGTACCCACT
 GGACAGTCCC CTGTTAAGAC CGATGATCAG GAATCCTCAC TCTTCCCCAG AATGGAGCGT
 GCAGCCTGGC CCCAACAGCC GCAGCATGAA ACGCCGTGGC AAGTTCTCTG CAGCAGGGTC
 TGTCCCTTCT TGCAGCAGCT ACTGGAAAGG TGGGAATGGG GAAGACAGTC AGCCTGCTCT
 TGGGATATCT GAGGGCAGGG TTGGAGTCAC CACCAGGACC TGGGGGAAGC ACAGGCACAA
 Y
 GGCCACAGCT GAGAGCTGAC CCAGGCCCCA GGATGGCCGA CCGCTGCCCC AGCAGTGGAG
 AAACACCCAC GTCGGTGTAG AATCAGGCCA GGCCAGCCAC AGGCTAACCC AGGAGCAGAC
 GGCTTGAGAG CAGGGAGTGG GGCGGCTCCA AGCTCAGCAG GCCTCATTTC TAGACAGGGA
 GAGGGGATGG TAGGGCAGGA CCCACATGTG ACACCTGAGA GCTACAAAGG AGGAGGCCAG
 GACACCCCCT GGGGGAGCAC TGGAGTGTTG GGTACAGCAA CAAGGCAATA TGGCCGTCTG

  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: rs10904559 was not linked to the human genome 36.3 because it aligned to more than 2 locations on the genome.
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
10NW_001837930.2526496678633minusAalt_assembly_8HuRefHuRefview300
10NW_924584.18802688026plusTalt_assembly_1CeleraCeleraview300
10NT_077567.373803123803plusTref_assemblyreferencereferenceview300
YNT_113974.129993157743368minusGref_parreferencePARview300

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_077567
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AL713922.12 NC_000010.9 BX322596.3

  Population Diversity back to top
There is no frequency data.

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterwith2hit
DoubleHit found by:  BCM_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .