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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs35135194          
refSNP ID: rs35135194
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:126/129
Map to Genome Build:36.3
Allele
Variation Class:DIP:
deletion/insertion polymorphism
RefSNP Alleles:-/C
Ancestral Allele:Not available
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 ss40665317 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs35135194 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
ss40665317ABI|hCV34521131fwd/-/Cccactcatgggatgtgagtgaggcctccccttggcagcaggccaggactgggggggtccc07/17/0507/17/05126Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs35135194|allelePos=301|totalLen=601|taxid=9606|snpclass=2|alleles='-/C'|mol=Genomic|build=126
 CTGGGTCTGC TGGTGACCCT CATGATGAGA TGCCACTCAT GCTTGTGGCA GCAGCAGAGG
 GCACCACCCA GGGTGGCACA CAGAGCCCAC CTGTTCATCC CAGTGATGCC AACGTGACTA
 CTTGGTCGAG GTCTTGTCTG CAGGATTTTC CGCTGCAAAG CTACATTCCC TTGTCATTAA
 TTTGTCCACA GAAATGGGAC CATGTTGACG CTCCATCCCT CACTGCCCTC ATCCACTGCA
 CGCTGTGTCC ACCAAGGTGA TTGGCTCTGT CCACTCATGG GATGTGAGTG AGGCCTCCCC
 N
 TTGGCAGCAG GCCAGGACTG GGGGGGTCCC TGAGTAGCTG AAACTTGTAG GTGCTCCCTG
 GGCACAGGGC TTCAGGGGCC AAGGCTTGTC TGCCCCACTG GGCAACTGTC CACCCCCTTA
 GCAGGACTTT GAGGACATCC CGGCGGCTGC TGGGCTCCCC GGGGGCAGGG TGGACACCCC
 AAACTGCTCC CTTTGTCTCC CAAGCCCCTC ACTTGGACAG AGGCTCCGCT TAGTGTCCTG
 GCCCGTCTCT GCCATGGCCA TTGAGTGTGG GGTGTGGCAG AAGGGGGCTG TCAGGGTCTC

  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:  rs35135194 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_001838339.22065438^2065439558579^558580minus-alt_assembly_8HuRefHuRefview300..300
16NT_037887.4576774^576775576774^576775plus-ref_assemblyreferencereferenceview300..300
16NW_926018.1553201^553202837551^837552plus-alt_assembly_1CeleraCeleraview300..300

  NCBI Resource Links back to top
Submitter-Referenced
dbSNP Blast Analysis
GenBank HTGS Finished:
Z98883.5

  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
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .