NCBI
dbSNP
Attention: This page will be retired!
This legacy RefSNP page contains old data from dbSNP build 151 (March 2018) and is no longer maintained.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.
Spacer gif

Spacer gif
Reference SNP (refSNP) Cluster Report: rs142997764                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:134/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqWith1000GenomeData
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:C/T (FWD)
Allele Origin:
Ancestral Allele:T
Variation Viewer:link to VariationViewer
Clinical Significance:NA
MAF/MinorAlleleCount:C=0.0004/2 (1000 Genomes)
C=0.0005/63 (TOPMED)
HGVS Names
  • CM000672.2:g.88668T>C
  • NC_000010.10:g.134608T>C
  • NW_003571043.1:g.78668T>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 ss335882917 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs142997764 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
ss3358829171000GENOMES|20100804_snps_7526458_chr10_134608fwd/C/Tgtctgggctaacctttaatttcttcttctagaagtgagataattggacaagacatctttt03/22/1103/22/11134Genomicunknown
ss13359129471000GENOMES|PHASE3_V1_48502662fwd/C/Tggctaacctttaatttcttcttctagaagtgagataattggacaagacat08/16/1408/16/14142Genomicunknown
ss1596744275EVA_DECODE|EVA_DECODE_10_124608_253_rs142997764fwd/BC/Tggctaacctttaatttcttcttctagaagtgagataattggacaagacat03/02/1503/03/15144Genomicunknown
ss1623797607EVA_UK10K_ALSPAC|EVA_UK10K_ALSPAC_10_134608_26806391fwd/C/Tggctaacctttaatttcttcttctagaagtgagataattggacaagacat03/04/1503/04/15144Genomicunknown
ss1666791640EVA_UK10K_TWINSUK|EVA_UK10K_TWINSUK_10_134608_26806391fwd/C/Tggctaacctttaatttcttcttctagaagtgagataattggacaagacat03/04/1503/04/15144Genomicunknown
ss2171932779HUMAN_LONGEVITY|HLI-10-88668-T-Cfwd/C/Tggctaacctttaatttcttcttctagaagtgagataattggacaagacat11/18/1611/18/16150Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs142997764|allelePos=51|totalLen=101|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=151
 CCAAAAAACA AAGCCAGCAG GTCTGGGCTA ACCTTTAATT TCTTCTTCTA
 Y
 GAAGTGAGAT AATTGGACAA GACATCTTTT ACAGGCAGCT CTAAAAGATT

  NCBI Resource Links back to top
Submitter-Referenced
GenBank
NC_000010
dbSNP Blast Analysis

  Population Diversity (Alleles in RefSNP orientation) . See additional population frequency from 1000Genome [here] back to top

Sample AscertainmentGenotypesAlleles
ss#PopulationIndividual
Group
Chrom.
Sample Cnt.
SourceHWPC
T
ss1335912947EAS 1008AF 1.00000000
EUR 1006AF 1.00000000
AFR 1322AF 0.001500000.99849999
AMR 694AF 1.00000000
SAS 978AF 1.00000000

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.001+/-0.0200000

  Validation Summary: back to top
Validation statusMarker displays
Mendelian segregation
PCR results confirmed
in multiple reactions
Homozygotes detected
in individual genotype data
byClusterbyFreqWith1000GenomeDataUNKNOWNUNKNOWNUNKNOWN