rs36426002 SNP Detail

Summary

• ID
  rs36426002
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  126
• Last Updated in dbSNP Build
  126
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr6:117455607 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CCTCTATTTC CTGGGAATTC CAGTAGAGGA GATTTATGTA
  AGCCTTGGTA GCAAGTTTCA TTCACAGCCT GGCGTCTCCT ATTGTGCATG CTTCATCTTC
  Y
  TATATAACGT GTAAACTGCA TCAAAGACTT CACTGAGTGA TATATGTTAC ACATGAACAA
  AACGGTTTCA ATTCAACATG GAAGTTTCAG AAAACGAACA                      
  
  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	CAST/EiJ	MOLF/EiJ
ss51408573	NES13706438	PERLEGEN	MM_PANEL2	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ
rs36426002					SNP	T	C

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
ss51408573	NES13706438	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:117455607 () rs orientation: forward

Symbol	Name	Function Class
Rr637326	regulatory region 637326	567 bp proximal