rs46153732 SNP Detail

Summary

• ID
  rs46153732
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr3:129475751 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        GCACA GGACCCAGGC CGGCAAAGTC
  C
  TTCCTTATCA GTAAGTGACC GGGTG                                      
  
  C = C
  

  
  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	LG/J	SM/J
ss135887731	ENSMUSSNP354897	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
ss320962761	CHEV_3_129385020	CHEVERUD	SCREENING_POP	f	SNP			C	C
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	LG/J	SM/J
rs46153732					SNP	C	C	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:129475751 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Egf	epidermal growth factor			Intron
				Noncoding-Transcript-Variant
Rr585059	regulatory region 585059			1855 bp distal
Rr585060	regulatory region 585060			1321 bp distal
Rr585061	regulatory region 585061			637 bp distal
Rr585062	regulatory region 585062			within coordinates
Rr585063	regulatory region 585063			345 bp proximal
Rr585064	regulatory region 585064			1357 bp proximal
Tssr35620	transcription start site region 35620			1183 bp downstream