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This legacy RefSNP page contains old data from dbSNP build 151 (March 2018) and is no longer maintained.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: rs56061456                 
RefSNP
Organism:human (Homo sapiens)
Molecule Type:Genomic
Created/Updated in build:129/151
Map to Genome Build:108/Weight 1
Validation Status:byCluster
Allele
Variation Class:SNV:
single nucleotide variation
RefSNP Alleles:C/T (FWD)
Allele Origin:
Ancestral Allele:C
Variation Viewer:link to VariationViewer
Clinical Significance:NA
NA
HGVS Names
  • CM000667.2:g.173260804C>T
  • NC_000005.9:g.172687807C>T
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 ss75321204 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs56061456 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
ss75321204ILLUMINA|ILMN_Human_1M_cnv10033PP1fwd/BC/Tcttgctttggtcaatagaatgtgatggaaaaggccaggtgtggtggctcatgcctgtaat08/28/0708/29/07129Genomicunknown
ss123453452ILLUMINA|HumanCNV370v1_C_cnv10033PP1fwd/BC/Tcttgctttggtcaatagaatgtgatggaaaaggccaggtgtggtggctcatgcctgtaat04/14/0904/15/09131Genomicunknown
ss159846013ILLUMINA|HumanOmni1-Quad_v1-0_B_cnvi0000026-126_B_F_1514265406fwd/BC/Tcttgctttggtcaatagaatgtgatggaaaaggccaggtgtggtggctcatgcctgtaat08/04/0910/01/09131Genomicunknown
ss168876387ILLUMINA|HumanCNV370-Quadv3_C_cnvi0000026-126_B_F_1514265406fwd/BC/Tcttgctttggtcaatagaatgtgatggaaaaggccaggtgtggtggctcatgcctgtaat10/01/0910/02/09132Genomicunknown
ss169137250ILLUMINA|Human1M-Duov3_B_cnvi0000026-126_B_F_1514265406fwd/BC/Tcttgctttggtcaatagaatgtgatggaaaaggccaggtgtggtggctcatgcctgtaat10/01/0910/01/09132Genomicunknown

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|rs56061456|allelePos=54|totalLen=111|taxid=9606|snpclass=1|alleles='C/T'|mol=Genomic|build=132
 CCCAGCCTGG GCTAATCTTG TGACTTGCTT TGGTCAATAG AATGTGATGG AAA
 Y
 AGGCCAGGTG TGGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCTG AAGCAGG

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

  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