rs48878635 SNP Detail

Summary

• ID
  rs48878635
• 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
  Chr1:154067193 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G TTCTTACAGT CTTTCTATCC TCTTTTACAT GATATTCTTT
  GAGCCATGGA ATAGTGGTGT GTAGTCTTGT TTAAGGTAAA GTAATCCATA GTCGCTTGCT
  Y
  TCTGTTCCAT GACTCTACAT TAGCCACTGT TTGCTGCAAG GGCCCCAGCT GGGAAAACTA
  CTGCTGAATT TTCTCTCTGT TACCTGAAGA GTAGCTTCCA G                    
  
  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
ss145757396	ENSMUSSNP5518503	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs48878635					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:154067193 () rs orientation: forward

Symbol	Name	Function Class
Rr420824	regulatory region 420824	730 bp distal