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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs308887          
refSNP ID: rs308887
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:79/129
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:A
Clinical Association:unknown
HGVS Names
NM_000842.1:c.2631-817A>G
NT_008984.17:g.505111T>C
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 ss1802206 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs308887 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
ss397013KWOK|OVLP-000621-234618fwd/TA/Gggtggaagtgcaaaggagaaagagagagaaggccttcaaaaaacttgtcagtccctcaat06/30/0010/10/0379Genomic99 %
ss722139SC_JCM|AC024733.5_222175fwd/TA/Gggtggaagtgcaaaggagaaagagagagaaggccttcaaaaaacttgtcagtccctcaat07/27/0010/10/0385Genomicunknown
ss945863KWOK|OVLP-000804-374071fwd/TA/Gggtggaagtgcaaaggagaaagagagagaaggccttcaaaaaacttgtcagtccctcaat09/01/0010/10/0386Genomic99 %
ss1802206KWOK|OVLP-000925-653226fwd/TA/Gggtggaagtgcaaaggagaaagagagagaaggccttcaaaaaacttgtcagtccctcaat10/05/0010/10/0387Genomic99 %
ss16097764SC_SNP|NT_008984.16_505111rev/BC/Tattgagggactgacaagttttttgaaggccttctctctctttctcctttgcacttccacc11/18/0311/22/03120Genomicunknown
ss38792076ABI|hCV569838fwd/TA/Gggtggaagtgcaaaggagaaagagagagaaggccttcaaaaaacttgtcagtccctcaat07/16/0507/16/05126Genomicunknown
ss88680396BCMHGSC_JDW|JWB-0455914rev/BC/Tattgagggactgacaagttttttgaaggccttctctctctttctcctttgcacttccacc02/26/0802/27/08129Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs308887|allelePos=595|totalLen=795|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=129
 AGAGCTGTCT TGACTGAAAA TAACAGACCC CCTAGTAACA GAGATCTTGG ATTACTTTGT
 GATGGGAAAC TACACCAGAA TCTCTTCATA TAACATTCCT ggccagacgc agtggctcac
 gcctgtaatc ccaacacttt aggaggctga ggcaggttga tcacttgagg tcagcagttc
 tagaacagtc ttaccaacat ggtgaaaccc cgtatctact aaaaatacaa aattagctgg
 gcgtggtggc gcatgcctac aatcccagct tctcaggaag ctgaggcagg agattcgctt
 gaatcccaga ggccgagggt gcagtgagct gagatggcgc cactgcactt cagcctgggc
 aacaagagca aaactccgtc taaaaaacaa aaaataaaaa aaaaaTCTTG AGTGTCAGGC
 CACATTCTCT GACCTTTGTA AAGTTTCTGA AAGAACGTCT GCAGCTTCAG AAGCTATTGT
 GTCAGCTTTT AGTGGTAAGG AGAGGTACTA GGGCGCTGAG GCTGAGGCAC CAATCACATC
 TTGAGAGTGG CTTTCAGACC CCATGGTGGA AGTGCAAAGG AGAAAGAGAG AGAA
 R
 GGCCTTCAAA AAACTTGTCA GTCCCTCAAT ATTCACCAGG ATCCTAATTT GAGATCACTC
 TGCTAAGTGC CGAAGGCATT ATACAGCACT CTCACTCATT GAACTGTTAT TCAAGTACAG
 AACTCAAAAT ACATTTGTGA GGTGAATTTC TGTGAAGTAA AGAAGCTCTC ATTAGAAATG
 TGTGTTCATT AAATTTTTAT

  GeneView back to top
GeneView via analysis of contig annotation: GRM5 glutamate receptor, metabotropic 5
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_008984->NM_000842
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_008984->NM_000842->NP_000833505111reverseintron

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs308887 maps exactly once on NCBI human chromosome 11
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
11NW_001838029.2127183284482447plusAalt_assembly_8HuRefHuRefview594
11NW_925129.1127518386388531plusAalt_assembly_1CeleraCeleraview594
11NT_008984.1750511187883137minusTref_assemblyreferencereferenceview594

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_008984 AC040976 AC040976.3
dbSNP Blast Analysis
GenBank HTGS Finished:GenBank HTGS Draft:
AP003120.4 AP002966.1

  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_SSAHASNP
UNKNOWNUNKNOWNUNKNOWN

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Revised: May 25, 2006 1:38 PM .