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BUILD 130
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Reference SNP(refSNP) Cluster Report: rs9786714          
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:119/130
Map to Genome Build:36.3
Allele
Variation Class:SNP:
single nucleotide polymorphism
RefSNP Alleles:A/G
Ancestral Allele:G
Clinical Association:unknown
HGVS Names
NM_002760.3:c.335+997T>A
NT_011896.9:g.4523623A>G
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 ss13607023 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs9786714 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
ss13607023WI_SSAHASNP|chrY.NT_011896.8_4581449fwd/TA/Gcaccatcttgctactacgcctctcttgtcccctcccatcttctgctttatctaggtccca11/05/0311/22/03119Genomicunknown
ss75012715ILLUMINA|ILMN_Human_1M_rs9786714fwd/TA/Gcaccatcttgctactacgcctctcttgtcccctcccatcttctgctttatctaggtccca08/28/0708/29/07129Genomicunknown
ss80538744HGSV|Cor18507_SNV_20070510.chrY_7216504fwd/TA/Gcaccatcttgctactacgcctctcttgtcccctcccatcttctgctttatctaggtccca11/23/0711/25/07130Genomicunknown
ss115581090ILLUMINA-UK|NA18507_000000242_NCBI36.1_chrY_7233143fwd/TA/Gcaccatcttgctactacgcctctcttgtcccctcccatcttctgctttatctaggtccca01/15/0901/15/09130Genomic99 %

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs9786714|allelePos=501|totalLen=701|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=130
 TGTCCTAGGG TAAGtgtgtt agtccattca ggctgctata acaaaggatc ttagactcgg
 taatttacaa atgacagaca tttgcctcat ggttctggag gctggaaagt ccaagatcaa
 gacacggtgg attcagtatc tggcgaggac ccgcttcctg gttcatagat ggcacctttt
 cactgtgtcc tcacatggtg gaaggggtga gggatctctc tggggtccct tttataaggg
 cactcgtccc attcatgaga ctccaccctc atgacctccc aaaggacaca ccacctaaca
 ccatcacctg tgggtgagga tccaacatag ggatttggga ggacacaaga aattcaggcc
 atTCCAGCAG GGTAATTCCA TTTCCACCCA GGTGCCTTAG ATGAGGATGT CCTTCGTGTC
 TCTCTTTTCC CTCTATGGGT GCCTTTTATC CAATTCCCAT GTCCTCTCGC CACCATCTTG
 CTACTACGCC TCTCTTGTCC
 R
 CCTCCCATCT TCTGCTTTAT CTAGGTCCCA TCTCTCTACC GTGATTTTCT GCACTGTACT
 TCCTCCTATC TGGTCTTTCC CTCCCACCCT TGCTCCCCTT GAAGACATCC TTCACCTTAT
 AGCCTCATTG ATCCTCCCCA AGTACCTCTG CAATGACCAG TCTCTCTCCA GTCATCCTCA
 GGAAGCTCCT GAAGTATCCC

  GeneView back to top

GeneView via analysis of contig annotation:  

View more variation on this gene (click to hide).
Include clinically associated: in gene region cSNP has frequency double hit
Assembly SNP to Chr Chr Chr position Contig Contig position Allele
Function mRNA Protein
mRNA to Chr Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via analysis of contig annotation: N/A.

GeneView via direct blast against RefSeq sequences (used when no gene model is available):

Function Chr mRNA Protein
SNP to mRNA Accession Position Allele change Accession Position Residue change
on assembly: is labeled at position on chromosome .

GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A


  Integrated Maps: back to top
Genome Build Chr Chr Pos Contig Contig Pos SNP to
Chr		 Contig
allele		 Group term Group label Contig label Neighbor
SNP		 Map Method
doesn't map to any assembly.

  NCBI Resource Links back to top
Resource
Submitter-Referenced
GenBank
NT_011896
dbSNP Blast Analysis

  Population Diversity back to top
There is no frequency data.

  Validation Summary: back to top
Validation status Marker displays
Mendelian segregation		 PCR results confirmed
in multiple reactions		 Homozygotes detected
in individual genotype data
byCluster UNKNOWN UNKNOWN UNKNOWN

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Revised: May 25, 2006 1:38 PM .