rs50595707 SNP Detail

Summary

• ID
  rs50595707
• Variation Type
  SNP
• Alleles
  A

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr12:63993828 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      G TCATGGTGAT TCCACCAGAG GTTCTTTTAC CCTTGAGAAG
  AGTTTTTGCT ATCCTAGGTT TTTTGTCATT CCAGATGAAT TTGCAGATTG CTCTTTCTAA
  A
  TCGTTGAAGA ACTGAATTGG AATTTTGAAG GGGATTGCAT TGAATCTATA GATTGCTTTT
  GGCAAGATAG CCATTTTTAC AATGTTGATC CTGCCAATCC A                    
  
  A = A
  

  
  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	DBA/2J
ss144586990	ENSMUSSNP3988505	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs50595707					SNP	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:63993828 () rs orientation: reverse

Symbol	Name	Function Class
Gm59626	predicted gene, 59626	1873 bp upstream