rs32761950 SNP Detail

Summary

• ID
  rs32761950
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:151326956 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GTGTGTGTGT GTGTGTGTGT
  GTGTGCGCGC ACGCGCGCGC GCGCGCATGT GTGCAATCAT TAGACCTGAG GCCTGGGGTG
  GAAGCACTCA GCCAGGGGAC TCAGGGAGGG CAGCTCAGGT GCCCTCTTGA GTGTTACCAC
  ATCCGGCCTC AGAGCCAGGG CGGGGTCGAG GGCTGGGAGT AGAGGGAAGG CTTCAGTGGG
  Y
  CCACAACTAG AAAGTTTCAC ATCTTATTCC CAGGTTCACA CAGATGTGGG CGCCTGCCAC
  TCAGAGATAA AACTCCTGCT GGGCAGGGTA CCCAGAGATA GCCCACACGT CCTCCCCAGA
  GCAGAGCAGG CAAGGAAGAT CAGAGGGCCT TGTCCAGCCC TTGCCAGTTT CTTTCCAGAG
  CAAGGACACT GAACTAGCGT                                            
  
  Y = C/T
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

  ---

SNP Assays
and
SNP Consensus

Strain alleles of submitted assays, and consensus values for this SNP

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	AKR/J	CAST/EiJ
ss46725285	NES11000086	PERLEGEN	MM_PANEL2	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	AKR/J	CAST/EiJ
rs32761950					SNP	C	T

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss46725285	NES11000086	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:151326956 () rs orientation: forward

Symbol	Name	Function Class
Camta1	calmodulin binding transcription activator 1	Intron
Rr377429	regulatory region 377429	6 bp upstream
Rr605550	regulatory region 605550	1827 bp distal