rs248686606 SNP Detail

Summary

• ID
  rs248686606
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:115975478 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTTATATTCA ACCACCTCAG
  AGACAAGATG AAGCATTTCA AGACTCTTAC ATGTCTTCCT TGTGCTTGTA CTAGATAATG
  TCCTCTAGAA ACAACTATTA TTCTCTCACC ACAGGTTTAC CCGTCCTTGA GCTTTATCTG
  GTGTTAATAC TTTCTTGTCT AGTTTATTTC ATTGATGTCT GTGTCTGCGA TGCCCACCCA
  Y
  GTTACTGTAT ATCATGGTAG CTTGCTCCTC TGGACTATTA GTATTATTCT ACTATTGGTG
  AGTAATTGTG CTGGTTTCAT CTTTGTTTAT TATGTTGGGG ATGAAGAGAT GGACCAGAGG
  TTACAAGAAC TGGCTACTCT TCCAGAGGAC ATGGATTCGA TTCCCAGCAC CCACCTGGCA
  GCTCACAACC ATCTGCAACT                                            
  
  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	LG/J	SM/J
ss320894510	CHEV_3_115884747	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs248686606					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:115975478 () rs orientation: forward

Symbol	Name	Function Class
Rr583660	regulatory region 583660	1026 bp distal