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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs874208          
refSNP ID: rs874208
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:86/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/T
Ancestral Allele:A
Clinical Association:unknown
HGVS Names
NM_021226.2:c.1869-1650T>A
NT_017696.14:g.460776A>T
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 ss1298270 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs874208 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
ss1298270TSC-CSHL|TSC0204367fwd/TA/Ttgctggctgcagctctggggtctccttcccgggccctccaaccttctaccctgaggctcc09/06/0010/10/0386Genomic95 %
ss15975604SC_SNP|NT_017696.14_460776fwd/TA/Ttgctggctgcagctctggggtctccttcccgggccctccaaccttctaccctgaggctcc11/18/0311/22/03120Genomicunknown
ss77272374HGSV|Cor12156_SNV_20070510.chr10_49326318fwd/A/Ttgctggctgcagctctggggtctccttcccgggccctccaaccttctaccctgaggctcc10/09/0710/12/07129Genomicunknown
ss1094085831000GENOMES|CEU.trio.12.15.2008_2342582_chr10_49326318fwd/A/Ttgctggctgcagctctggggtctccttcccgggccctccaaccttctaccctgaggctcc12/15/0812/16/08130Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs874208|allelePos=448|totalLen=831|taxid=9606|snpclass=1|alleles='A/T'|mol=Genomic|build=130
 CTGAACAATG ATGTCCTCcc ctaagtccat tctttttctc ggtcccatat ctgatcagtt
 agcaaaacct tttggctcta ccttcaaaat atgctcagca cctggccgct tcccccacct
 ccacctgctg ccccataggg ccacaccccc cataggtcag gcctagaccc ccacacctcc
 taactggtct gttctgccct tgtcccctgg caagctctgc tcggcatggc acccaggtgc
 acctgtcaaa gtgcccaatg tgccaaaccc tccagcggct tctcacttca ttctcatctc
 actccacgaa aaaccagagc attgcccagg ccaaaaggcc ccacccattg ccccctcccc
 acacatctcc agtccccagc ccctgactct cccccACTAC AGGGGTCTTG GGGTCAGTGC
 TGGCTGCAGC TCTGGGGTCT CCTTCCC
 W
 GGGCCCTCCA ACCTTCTACC CTGAGGCTCC TCTCCGCTCC CCTCCATGCT GCTCTATGTT
 CCCCTCCTTC ATCTCCCTTT TAACACACCG TGTATTTTTA AAAATGTATC GTGCTTATGG
 TCTTTGTCTC CCTGCAACCC AAATAAGAAT GGGGACAGAG ATTTTGATCA GTTTTCACCC
 CAACTGTGGC CACCTGCACA GCATCTGGTA CTTCACAGAA AACAGGTTCT CTTTTGGGAA
 TGCACGAAGG AAGGCTGACT CCAGCAGGGC CCTGGGGAGG GGCTCTGACC AGATCCCTGG
 GAGCCAGACA AGGCCAGCTA CCCCACCCCC ACCCGATGGC CCATACTTCA GAGACAGGAA
 CACATTCCCC AATCACTGCT GGA

  GeneView back to top
GeneView via analysis of contig annotation: ARHGAP22 Rho GTPase activating protein 22
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_017696->NM_021226
svfunction
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_017696->NM_021226->NP_067049460776reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs874208 maps exactly once on NCBI human chromosome 10
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
10NW_924685.128437343242219plusAalt_assembly_1CeleraCeleraview447
10NW_001837974.128705943921136plusAalt_assembly_8HuRefHuRefview447
10NT_017696.1446077649326318plusAref_assemblyreferencereferenceview447

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_017696
dbSNP Blast Analysis

  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
with2hit
DoubleHit found by:  BCM_SSAHASNPNCBI
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .