rs108704598 SNP Detail

Summary

• ID
  rs108704598
• Variation Type
  SNP
• Alleles
  C/G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:175308122 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        AGACT CTCCAGGAAT AAACAAATGG
  S
  TAATAAGTGT AGAAAAAGAT GCCCA                                      
  
  S = C/G
  

  
  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	129X1/SvJ	A/J	LG/J	SM/J
ss146321567	ENSMUSSNP3259824	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	G
ss320151361	CHEV_1_177410687	CHEVERUD	SCREENING_POP	f	SNP			C	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	LG/J	SM/J
rs108704598					SNP	C	G	C	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:175308122 () rs orientation: forward

Symbol	Name	Function Class
Rgs7	regulator of G protein signaling 7	within coordinates
Tssr15391	transcription start site region 15391	1132 bp upstream
Tssr15392	transcription start site region 15392	1011 bp upstream