rs49926966 SNP Detail

Summary

• ID
  rs49926966
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:75650105 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTCCAATGAA AGAAACAGAT
  CAGTGATCAA CCTCCCAAGT AGCTGGGATT ATGGATGTGG TCATCATGGC CAGCAAGAAT
  TATATTTTTA TGTGTATGAC AAATAGATTG ATTTGAAGTT AGTTTTGACT GAAATCCTTT
  CCCCAATGTC TAGTTCTCTA AAGCAGGAAT ATCTATGGGA GAGTTTTTTT ATGCTTTTGG
  Y
  AAACAGCAGT TTCTCAGCCC CAGAAGCACT GACAGGGAAG AACAGATGAG ACTCATCACC
  TCCCATTCCT TTGAGCATCT TTAAACAGTT AATGTTTCTT AGGAGGGGTG CATCATTTTC
  TTCACTGAGA AAGGCACTGA TAAGTTATCC ATGCTCTAGT AAGTAAACTC TTACCCACAC
  TCACTTGAGA AACTCAAATC                                            
  
  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	A/J	DBA/2J
ss135330165	ENSMUSSNP7232529	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs49926966					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:75650105 () rs orientation: forward

Symbol	Name	Function Class
Rr397722	regulatory region 397722	652 bp upstream