rs46615077 SNP Detail

Summary

• ID
  rs46615077
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:166492925 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AGATGACTGC AGTACACATC TTAGAGACTT CCCTGAAACA
  AGATACCATC CTGCGATGCT ACCTGTGGCT CCCCGGGGCC CTGTCCACTG CTGGACCACG
  Y
  AGTCCCTCAG CATCCATCAA GTTCCCTCAT CCCAGTAATA AGAGTAATTA TGACATACAT
  CAAGGATGCA GGAAACAGTA AGCTCATCGC TCCATGGCT                       
  
  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	A/J	DBA/2J
ss148257492	ENSMUSSNP6075096	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs46615077					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:166492925 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Prex1	phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 1			Intron
				Noncoding-Transcript-Variant
Rr570327	regulatory region 570327			158 bp distal
Rr570328	regulatory region 570328			346 bp proximal
Rr570329	regulatory region 570329			508 bp proximal
Rr570330	regulatory region 570330			1778 bp proximal