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Reference SNP (refSNP) Cluster Report: rs267608664                 ** With Uncertain significance allele **
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:137/151
Map to Genome Build:108/Weight 1
Validation Status:byClusterbyFreqWith1000GenomeData
Citation:PubMedLitVarNEW
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:A/C/T (FWD)
Allele Origin:C:germline
T:unknown
Ancestral Allele:C
Variation Viewer:link to VariationViewer
Clinical Significance:With Uncertain significance allele [ClinVar]
MAF/MinorAlleleCount:T=0.00003/3 (ExAC)
T=0.0003/1 (1000 Genomes)
T=0.00006/7 (TOPMED)
HGVS Names
  • CM000685.2:g.18646060C>A
  • CM000685.2:g.18646060C>T
  • NC_000023.10:g.18664180C>A
  • NC_000023.10:g.18664180C>T
  • NC_000023.11:g.18646060C>A
  • NC_000023.11:g.18646060C>T
  • NG_008475.1:g.225456C>A
  • NG_008475.1:g.225456C>T
  • NG_008659.3:g.36389G>A
  • NG_008659.3:g.36389G>T
  • NM_000330.3:c.326+1131G>A
  • NM_000330.3:c.326+1131G>T
  • NM_001037343.1:c.2767C>A
  • NM_001037343.1:c.2767C>T
  • NM_003159.2:c.2767C>A
  • NM_003159.2:c.2767C>T
  • NP_001032420.1:p.Arg923Cys
  • NP_001032420.1:p.Arg923Ser
  • NP_003150.1:p.Arg923Cys
  • NP_003150.1:p.Arg923Ser
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 ss538296855 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs267608664 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
ss538296855CHWRETT|CDKL5: c.2767C>Tfwd/BC/Tcagagacaccattctggaccccaagatagagcttcatgttaaggacgacagaacaacaag08/08/1208/08/12137Genomicunknown
ss15536876661000GENOMES|PHASE3_chrX_461490fwd/BC/Tacaccattctggaccccaagatagagcttcatgttaaggacgacagaaca08/16/1401/30/15144Genomicunknown
ss1694468893EVA_EXAC|EXAC_0.3.X:g18664180c>tfwd/C/Tacaccattctggaccccaagatagagcttcatgttaaggacgacagaaca03/04/1503/04/15144Genomicunknown
ss1694468894EVA_EXAC|EXAC_0.3.X:g18664180c>afwd/A/Cacaccattctggaccccaagatagagcttcatgttaaggacgacagaaca03/04/1503/04/15144Genomicunknown
ss2316006016HUMAN_LONGEVITY|HLI-X-18646060-C-Tfwd/C/Tacaccattctggaccccaagatagagcttcatgttaaggacgacagaaca11/18/1611/18/16150Genomicunknown
ss2745323955GNOMAD|exomes_rs267608664fwd/A/C/Tacaccattctggaccccaagatagagcttcatgttaaggacgacagaaca05/17/1705/17/17151Genomicunknown
ss3606391057TOPMED|TOPMed_freeze_5?chrX:18,646,060fwd/C/Tacaccattctggaccccaagatagagcttcatgttaaggacgacagaaca10/07/1710/07/17151Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs267608664|allelePos=51|totalLen=101|taxid=9606|snpclass=1|alleles='A/C/T'|mol=Genomic|build=151
 GTGGATGTGA TGGCAGAAGA CAGAGACACC ATTCTGGACC CCAAGATAGA
 H
 GCTTCATGTT AAGGACGACA GAACAACAAG GTAGAGTCTG GGCCCCGCAT

  NCBI Resource Links back to top
Submitter-Referenced
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.
SourceHWPA
C
T
ss1553687666EAS 1008AF 1.00000000
EUR 1006AF 1.00000000
AFR 1322AF 1.00000000
AMR 694AF 1.00000000
SAS 978AF 0.998999950.00100000
ss1694468893ExAc_Aggregated_Populations121411AF 0.999925850.00007413
ss1694468894ExAc_Aggregated_Populations121403AF 0.000008240.99999177

SummaryAverage
Het.+/- std err:
Individual
Count
Founders
Count
Individual
Overlap
Genotype
Conflict
0.000+/-0.0090000

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

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