rs29767986 SNP Detail

Summary

• ID
  rs29767986
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:152787891 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTGGGAGAAG AGCCCCAAAG
  GGCAAGGCTT CAGCCCGAGT CCATCTCAAG CTCCAGGTAC CCGTGCTAGT GAATCAAACA
  ACCCCCTGTT TTCCAGAGCC CCTGCCATCA CCGGGTTCTG TCCCACATCC TCATCCTCGC
  AAGCACCCTT GACTCGTCAA GGATGCTGTA GCCAAAGCTC AGAGAGGATA AATGATTTTC
  R
  TCAAGGTCAC AGAGCAGTAA ATGGCCAAGC CTGGCTGCAA ACCAGGTGTC TGAACTGCAA
  GCCAGGATTC AGGTCGAGTC TGACCCTCAA ATCTGCTGTA CACCCGGTCC CGAGAGGCAG
  GACACTCTCT CCCCGTCATA GGGGAGGAGA CTGATGCTCC AGAGAGAGCC GAATAGGGAC
  ATGCTACAAG GACATGGTTG                                            
  
  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	A/J	C57BL/6J	DBA/2J
ss45359363	mCV23536542	ABI	CRAMUS_MOUSE	f	SNP	A	G	G
ss147977600	ENSMUSSNP3056174	ENSEMBL	ENSEMBL_Sanger	f	SNP	A		G
SNP Consensus Information
SNP					Consensus Type	A/J	C57BL/6J	DBA/2J
rs29767986					SNP	A	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:152787891 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dusp15	dual specificity phosphatase-like 15			Intron
				Noncoding-Transcript-Variant
Rr567515	regulatory region 567515			1147 bp proximal