rs263870198 SNP Detail

Summary

• ID
  rs263870198
• 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
  Chr3:109762382 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    AACACTGGA TGCTTAGAAT TCAGGCTCTT
  CTTCACTCTG TGTGGTGTGG TTTTTTGAGG TACTGCCAGA TGAGTCACTC TTTATTCCAT
  GTCTGTAAAA ATGGTAATTG CTCAGAAGAG ATTTTTAAAC TGCTCATTTG AATAAGGAGT
  Y
  TTGAAATTGA ATATATCTGA GCACCAAGGG ATGCCCATTA ATTCATTTCA AAATGTTATT
  TTCTCCTAAT GGTCCCTATT TTAATGTCAA AAGTTCCTTG CTTTGGGTTG TCTGCAGAGA
  ACTGAAGAAC TTAGAAAACC CACTACATCC                                 
  
  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
ss320870675	CHEV_3_109657984	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs263870198					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:109762382 () rs orientation: forward

Symbol	Name	Function Class
Ntng1	netrin G1	within coordinates
Rr65057	regulatory region 65057	1782 bp distal