rs48957930 SNP Detail

Summary

• ID
  rs48957930
• Variation Type
  SNP
• Alleles
  A

• 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
  Chr10:52262642 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G ATTCCATTCC CACTTAGGGT TCTGCAAGTG TCTGCTATAG
  TGCTTTGTGG TCGCCATATG AAACACCTTA GCAGGTAAGC CCTACGCTGG GACCTGCTTA
  A
  GTTGAAATCT CAGATGCTAG CTTGGGAGAT GGCTCAGCAA ATAAAATGCT TGGTGACCAA
  GAATGAAGGC CTCAGTTGGG ACCCTTAACA CCTCATAAAA G                    
  
  A = A
  

  
  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
ss147112164	ENSMUSSNP4078170	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs48957930					SNP	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:52262642 () rs orientation: forward

Symbol	Name	Function Class
Gm67152	predicted gene, 67152	within coordinates
Rps19-ps10	ribosomal protein S19, pseudogene 10	1453 bp upstream
Rr431355	regulatory region 431355	963 bp distal
Rr431356	regulatory region 431356	1070 bp distal