rs107664731 SNP Detail

Summary

• ID
  rs107664731
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:150310749 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T CATAAGATCC TTGCTTTTAA TAGTCGAAGT GTATCCCATT
  GTGTAAATGA AACACATTTT CTGTAATCAT TCTTTGGTTG AGGGACATCT GGGTTGTTTC
  T
  AGCTTCAGCC TATTATGAAT AAAGCTGCTA TGAAGGTAGT GGAGCACGTG TCCTTTTGGT
  ATAGGTGAGC ATCTTTTGGG TATATGCCCA AGAGCGCTAT A                    
  
  T = 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	A/J
ss147948913	ENSMUSSNP5092372	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	A/J
rs107664731					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:150310749 () rs orientation: forward

Symbol	Name	Function Class
Cpgi12405	CpG island 12405	1245 bp proximal
Gm14127	predicted gene 14127	582 bp downstream
Rr567041	regulatory region 567041	1229 bp proximal