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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs16821690          
refSNP ID: rs16821690
Organism:mouse (Mus musculus)
Molecule Type:Genomic
Created/Updated in build:123/128
Map to Genome Build:37.1
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:C/T
Strain:not submitted
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 ss24777426 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs16821690 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
ss24777426ROCHEBIO|Pttg1_JC10507_7byFreqfwd/BC/Tagtgctaggattaaaggcatgtgccaccacgccnggccttgtnaggcattcaccagattg05/28/0408/05/04123GenomicTunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs16821690|allelePos=386|totalLen=483|taxid=10090|snpclass=1|alleles='C/T'|mol=Genomic|build=123
 ATGTATGTTG TATTAAAAAA GCATTTGTGC ATATGTTCAG ATNNTGAATA CTTAACCNAC
 CCCTGATTGG TATTTTTTGG TGTTAGGAGA CGCCACTGTT CTCCTTTGGA AGTAGACCCC
 TCAATGTGTC CCTTTTTGTG GCTGTTAGCT AGTGACAGTT ATTAGATCTC TTANTTAAGG
 AGTCACTCCC AGCTCATTTA GTATTTGTTA GGCATTCTTt ttttgttttt ttttgttttt
 gtttttgttt tttttttttt gagatagggt ttctctgtat agccctngct gtcctggaac
 tcactttgta gancaggctg gccttgaact caaatccacc tgcctntgcc tcccaagtgc
 taggattaaa ggcatgtgcc accac
 Y
 gccnggcCTT GTNAGGCATT CACCAGATTG GTTTAGTTCT AATGACTTTA GTATTCAGTA
 ACNAGAATTG AAAGGCTCTG AGTCTTTGAG AACNGTC

  GeneView back to top
GeneView via analysis of contig annotation: Pttg1 pituitary tumor-transforming 1
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
CeleraNW_001030461->NM_013917
function
C57BL/6JNT_096135->NM_013917
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
CeleraNW_001030461->NM_013917->NP_038945505410reverse3' near gene
C57BL/6JNT_096135->NM_013917->NP_0389458738297reverse3' near gene

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs16821690 maps exactly once on NCBI mouse chromosome 11
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
11NT_096135.5873829743233419minusAref_strainC57BL/6JC57BL/6Jview385
11NW_001030461.150541048048422minusAalt_assembly_1CeleraCeleraview385

  NCBI Resource Links back to top
Submitter-Referenced
dbSTS
RPAMMSEQ0038999
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank STS:
AL670472.7 BV161468.1

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
T/T
ss24777426RPAMM 6IG 1 2

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.444+/-0.1573300

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

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Revised: May 25, 2006 1:38 PM .