rs27362303 SNP Detail

Summary

• ID
  rs27362303
• 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
  Chr2:149774898 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGAACCCTAG ATAAATGACA
  TAGGTCTAGG AATGGTGGCC TGTGTGTCCA TACCAGAGGC CAGCTTCATC AAACCTGCTA
  CGGATCCCAA CCAGATTCCT GGGCTAGTTG AGGCAGGCTC AGATGAGCTT GGCCTCTAAG
  GTCTCCAAAG GTACTGTCCA GAATGCAGAT GAGGGTACAT GAGGCTTTGG AGAAAGACTT
  R
  GGTTAGGAAT CTATGGTGAG TGCCATCTGC TCCCACCTAT ATAAGACCAC CCTGGATGAT
  CTCTGCTTCT TCACATAGTC TGCAGTGAAG CCCTGTCTTC TTCTAGGTAG AACATGTTGT
  GGCCAAGGAG ATTAGAGAAT TCAGACTCTC AGTTCACATA TTAAGCTGCT CTTTATGTGG
  TAAGAATCTC TTAGACTTAG                                            
  
  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	CAST/EiJ	MOLF/EiJ	NZW/LacJ	PWD/PhJ
ss37570422	NES08921961	PERLEGEN	MM_PANEL2	f	SNP	G	G	A	G
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ	NZW/LacJ	PWD/PhJ
rs27362303					SNP	G	G	A	G

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss37570422	NES08921961	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:149774898 () rs orientation: forward

Symbol	Name	Function Class
Rr567007	regulatory region 567007	542 bp proximal
Rr567008	regulatory region 567008	1063 bp proximal
Syndig1	synapse differentiation inducing 1	Intron