rs32760716 SNP Detail

Summary

• ID
  rs32760716
• 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
  Chr4:151322483 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTGAAAACTG TATAACTATA
  TAAGTATCCC TCAGGAGTCT TTAACTTGAT GCACTTTTTC ATCCTCAACT GGCCTGTGGC
  TCCCGCTTGT AATCTGGGAA GGGTTAGCAC CAGACCCATG CATCTAGGTT GCCTCCTTGG
  GAGGCCGAGG CAAGAGAGGG GGCTGATCCA CAAGTCTGTG AGGCATAAGC CATGCAGTCC
  Y
  TTCTGCATCG TGGACATGTG CTCCTGGAAG TCAGGGCATC ACTGAACTCT CGGCCTAGGG
  TGGGAAGGGG TCTGACCCAT ACCTGGGACG TAGGACTGTT GAAACTCTCC TCAGCTGGGG
  CCACTGTTCT GGGCAGGCTG GTTTGTTCAG TGGTTTCATG ACAAGAGTGT CAGCTAGTCC
  TGATCCTCTG GTGAAACCTG                                            
  
  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
ss46725267	NES11000274	PERLEGEN	MM_PANEL2	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	AKR/J	CAST/EiJ
rs32760716					SNP	T	C

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
ss46725267	NES11000274	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:151322483 () rs orientation: forward

Symbol	Name	Function Class
Camta1	calmodulin binding transcription activator 1	Intron
Rr605547	regulatory region 605547	1066 bp proximal
Rr605548	regulatory region 605548	1513 bp proximal