rs262167547 SNP Detail

Summary

• ID
  rs262167547
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr4:102295471 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CAGATATACT AAGTGGGCAA
  GTATATTCTA ACTTCTGAGT TTAATATTTT AATATATTTA TGTAATATTT TTATATATCA
  TGTTTTTTAT GTTTATAGGG AAAAGAACAT TTTTTATTTA TATTTTTGTA TTTCTAGGAC
  ATATCCCAAA TAAAATCATA GACTCACATT TACTAAATGT TTGAAATTTA ATTTACGGAT
  R
  CTTATAGCAT TCACTAAAAA TTATGTATGT GAAAATATTT CATCAACTGT TGAGCTCAAC
  ATAACTTGAA TTATTACCAC TCATAATTTT TAAATGTTCA GTATTAGCTA TGAATTTAAA
  AAATTGCTGA AAACAGTTTG ATGTGCTCTT GTCTCTAGGA GTGCATATTA TCCACTTGTT
  ATGGATCTTA TAAAATGTTA                                            
  
  R = A/G
  

  
  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
ss321233620	CHEV_4_102110879	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs262167547					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:102295471 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Pde4b	phosphodiesterase 4B, cAMP specific			Intron
				Noncoding-Transcript-Variant
Rr596244	regulatory region 596244			1130 bp proximal
Rr596245	regulatory region 596245			1905 bp proximal