NCBI
dbSNP
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This legacy RefSNP page contains old data from dbSNP build 151 (March 2018) and is no longer maintained. Please update your links and bookmarks to use the re-designed RefSNP Report page.
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Reference SNP (refSNP) Cluster Report: rs9651492                 ** With Uncertain significance allele **
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:119/151
Map to Genome Build:108/Weight 1
Validation Status:byCluster
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/C/G (FWD)
Allele Origin:A:germline
G:germline
Ancestral Allele:G
Variation Viewer:link to VariationViewer
Clinical Significance:With Uncertain significance allele [ClinVar]
NA
HGVS Names
  • CM000672.2:g.87933216G>A
  • CM000672.2:g.87933216G>C
  • NC_000010.10:g.89692973G>A
  • NC_000010.10:g.89692973G>C
  • NC_000010.11:g.87933216G>A
  • NC_000010.11:g.87933216G>C
  • NG_007466.2:g.74778G>A
  • NG_007466.2:g.74778G>C
  • NM_000314.4:c.457G>A
  • NM_000314.4:c.457G>C
  • NM_000314.6:c.457G>A
  • NM_000314.6:c.457G>C
  • NM_001304717.2:c.976G>A
  • NM_001304717.2:c.976G>C
  • NM_001304718.1:c.-294G>A
  • NM_001304718.1:c.-294G>C
  • NP_000305.3:p.Asp153Asn
  • NP_000305.3:p.Asp153His
  • NP_001291646.2:p.Asp326Asn
  • NP_001291646.2:p.Asp326His
  • NP_001291646.2:p.Asp?His
  • NW_013171807.1:g.149008G>A
  • NW_013171807.1:g.149008G>C
Links
SNP Details are organized in the following sections:
GeneView Map Submission Fasta Resource Diversity Validation

  Integrated Maps (Hint: click on 'Chr Pos' to see variant in the new NCBI variation viewer) back to top

  GeneView back to top

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


  Submitter records for this RefSNP Cluster back to top
The submission ss13439507 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs9651492 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
ss13439507SC_SNP|NT_030059.10_8131521fwd/BC/Gggcaaatttttaaaggcacaagaggccctaatttctatggggaagtaaggaccagagaca10/23/0310/31/03119Genomicunknown
ss2137511272CLINVAR|SCV000541610_398053fwd/TA/Gggcaaatttttaaaggcacaagaggccctaatttctatggggaagtaaggaccagagaca04/28/1705/05/17150Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs9651492|allelePos=201|totalLen=401|taxid=9606|snpclass=1|alleles='A/C/G'|mol=Genomic|build=150
 CACAATATCC TTTTGAAGAC CATAACCCAC CACAGCTAGA ACTTATCAAA CCCTTTTGTG
 AAGATCTTGA CCAATGGCTA AGTGAAGATG ACAATCATGT TGCAGCAATT CACTGTAAAG
 CTGGAAAGGG ACGAACTGGT GTAATGATAT GTGCATATTT ATTACATCGG GGCAAATTTT
 TAAAGGCACA AGAGGCCCTA
 V
 ATTTCTATGG GGAAGTAAGG ACCAGAGACA AAAAGGTAAG TTATTTTTTG ATGTTTTTCC
 TTTCCTCTTC CTGGATCTGA GAATTTATTG GAAAACAGAT TTTGGGTTTC TTTTTTTCCT
 TCAGTTTTAT TGAGGTGTAA TTGACAAGTA AAAATTATAT ATAAATACAA TGTATAATAT
 GATGTTTTGA TGTATGTGTA

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NT_030059
dbSNP Blast Analysis
UniGene Cluster ID
500466
3D structure mapping
NP_000305  

  Population Diversity (Alleles in RefSNP orientation) 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
byClusterUNKNOWNUNKNOWNUNKNOWN