rs51341322 SNP Detail

Summary

• ID
  rs51341322
• Variation Type
  SNP
• Alleles
  G/T

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr3:117659998 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        GTGGC TTTTTGAAAA CTCAACCCAG
  K
  TTGCTTTGCT TCCCATTCTC CCTGC                                      
  
  K = G/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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss135694675	ENSMUSSNP5899997	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	T	G
ss320900594	CHEV_3_117569267	CHEVERUD	SCREENING_POP	f	SNP				T	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs51341322					SNP	G	T	G	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:117659998 () rs orientation: forward

Symbol	Name	Function Class
Rr583873	regulatory region 583873	283 bp distal
Rr583874	regulatory region 583874	549 bp proximal
Snx7	sorting nexin 7	Intron