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BUILD 129
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Reference SNP(refSNP) Cluster Report: rs10404335          
refSNP ID: rs10404335
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:119/129
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
NM_030901.1:c.123G>A
NP_112163.1:p.G41G
NT_011295.10:g.6254846C>T
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 ss69375182 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs10404335 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
ss14695007BCM_SSAHASNP|chr19.NT_011295.10_6254847fwd/BC/Ttgagattgtggccaggatgatgagcagattccgagcacagtgaccaggtacatggacaga11/10/0311/22/03119Genomicunknown
ss48412567APPLERA_GI|hCV25653506byFreqfwd/BC/Ttgagattgtggccaggatgatgagcagattccgagcacagtgaccaggtacatggacaga09/28/0511/03/06126Genomicunknown
ss69375182SI_EXO|NT_011295.10_6254847fwd/BC/Ttgagattgtggccaggatgatgagcagattccgagcacagtgaccaggtacatggacaga04/12/0704/12/07127Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs10404335|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=127
 GGATTTCCAA GTCTGTGCAG AAGGACAGCC ACAATACCAT TAAGCTTTGT GACAAGGAAT
 TCAGGGCAGC AATCATCCAG GATGCCAGAA CCAGGAGTCC ACAGAGCCGA GGGTTCATGA
 TGACTGTGTA GTGCAGAGGA TGACAGATGG CCACAAACCG ATCATAGGCC ATCACAGCCA
 GGAGTAAGCT GTCTAACCCT CCAAAAAGTA CAAAAAAGCA CATCTGGGTG ATGCAGCCTG
 CATAGGTGAT GACTCTGCTC TGTGTCTGGA TGTTAATGAG CATCTTTGGG ATTGTAGTGG
 AGATGAAACA GATGTCTGCA AAGGACAGGT TGGAGAGGAA GAAGTACATG GGGGTGTGGA
 GGTGGGAGTC TGAGATTGTG GCCAGGATGA TGAGCAGATT
 Y
 CCGAGCACAG TGACCAGGTA CATGGACAGA AACAGCCCAA AGAGGAAGGG CTGCAATTCT
 GGTTCCTCAG AAAGTCCCAG AAGAACAAAT TCTGAAATCC CTGTGTCATT CTCTGGTTCC
 ATCTTTTTTT TTCTATTTAT TTATTTATTT ATTTATTTAT TTATTTATTT ATTAACATAG
 ACAGGGTCTC TCACTCTGTT GCCAACGCTG GTCTGAACCT CCTGGACTCA TGCGATCCTC
 CCACTTCAGC CTACAAAAGT GCTGAGATTA TAGGCATAAG CCATTGTGCC CAGGCTTGGT
 TGCATCTTTT CAATGTGACT ACCAAAAAGA GAGAGAATAT GACAATGTAA TTATGCATTA
 CAAACCTATC AGAAATTCTC TCATTTATAC TCCGGAGTCA

  GeneView back to top
GeneView via analysis of contig annotation: OR7A17 olfactory receptor, family 7, subfamily A, member 17
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_011295->NM_030901
function
"
Group
label
Contig-->mRNA-->ProteinContig
position
mRNA
orientation
mRNA
pos
FunctiondbSNP
allele
Protein
residue
Codon
pos
Amino acid
pos
referenceNT_011295->NM_030901->NP_1121636254847reverse123synonymousAGly [G]341
contig referenceGGly [G]341

GeneView: no link established by BLAST analysis of mRNA sequences
  Integrated Maps: back to top
NCBI MapViewer:  rs10404335 maps exactly once on NCBI human chromosome 19
ChromosomeContig
accession
Contig
position
Chromosome
position
Hit
orientation
Contig
Allele
Assembly
Type
Group
label
Contig
label
Neighbor
SNP
SNP_flank
position
19NW_001838484.128440314560023plusCalt_assembly_8HuRefHuRefview400
19NT_011295.10625484714853045plusCref_assemblyreferencereferenceview400
19NW_927195.1610404014887794plusCalt_assembly_1CeleraCeleraview400

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_011295.10
dbSNP Blast Analysis
NCBI RefSeq NM (mRNA):
NM_030901.1
UniGene Cluster ID
247717
3D structure mapping
NP_112163  

  Population Diversity back to top

Sample AscertainmentGenotype Detailnew.gifAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceC/C
C/T
T/T
HWPC
T
ss48412567AGI_ASP populationmultiple 66IG 0.545 0.273 0.182 0.050 0.682 0.318

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.434+/-0.169333300

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

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Revised: May 25, 2006 1:38 PM .