rs211758726 SNP Detail

Summary

• ID
  rs211758726
• 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 | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr3:10345869 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAAAAGACTT AGAAGAGGGG
  AGGAGGAATA GGGACTACAG TTACAACGTA CAGCCTTAAG TTGGTTTTCA AAGACTGCTC
  ATAGCTGAGA CTGGATAAGC AATTGCTCAG ATGTTACCAG TAGAAGGAGA AACTGCTAGC
  CACAGATTTG TTTCAAAAGT GGTTTTGCAG GGATGTATGT TTATTGCTCT GCTTTGTGGC
  Y
  CTCCTGCTGG TAGCAAATTG TGCCTGTCTT CAAAGTGTCC AGCTTGCCTT TTTAACTTGC
  CTGCATCTGT CGGTTTTCTT CCACACGCTC TTCCTCCTGT GAGATCCACT TCAGTCATCC
  AGTCATTCAG TCAGTGCGGA TTCCCTACCC TCCTAAGTCC CACACTCTGG GGGATGCTTG
  GAATGCAATG GTGAGCATAG                                            
  
  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
ss320653241	CHEV_3_10280809	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs211758726					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:10345869 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Fabp12	fatty acid binding protein 12			Intron
				Noncoding-Transcript-Variant
Rr573601	regulatory region 573601			552 bp proximal