rs48697362 SNP Detail

Summary

• ID
  rs48697362
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr7:61695210 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T TATGGACCAG TAGCTCTCCT GTCTCTGTTA TATACTGAAA
  GCTGAGATGT TTATGGACCA GTAGCTCTCC TGTCTCTGTT ATATACTGAA AGCTGAGATG
  Y
  TTATGGACCA GTAGCTCTCC TGTCTCTGTT ATATACTGAA AGCTGAGATG TTTATGGAAC
  AGCAGCTCTC CTGTTTCCTG TTATATACTG AAGGCTGGGA T                    
  
  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
ss144765107	ENSMUSSNP2969266	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs48697362					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:61695210 () rs orientation: forward

Symbol	Name	Function Class
Gm72932	predicted gene, 72932	within coordinates
Mir344f	microRNA Mir344f	719 bp downstream
Rr647584	regulatory region 647584	454 bp proximal
Tssr72743	transcription start site region 72743	782 bp downstream