rs217558676 SNP Detail

Summary

• ID
  rs217558676
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr6:119466730 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        AATTT AGAGGCAGAA AACAGACAAA
  Y
  GTGGTTTCCT TTGCTTTTAC TTAAT                                      
  
  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	LG/J	SM/J
ss321928163	CHEV_6_119439787	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs217558676					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:119466730 () rs orientation: forward

Symbol	Name	Function Class
Rr637698	regulatory region 637698	39 bp proximal
Rr637699	regulatory region 637699	139 bp proximal
Rr637700	regulatory region 637700	738 bp proximal
Rr637701	regulatory region 637701	1173 bp proximal
Wnt5b	wingless-type MMTV integration site family, member 5B	Intron