rs108466112 SNP Detail

Summary

• ID
  rs108466112
• Variation Type
  SNP
• Alleles
  A

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

Genome Location and Flanking Sequence

• Location
  Chr2:128160650 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T CACTGAAGAA AATCATAATT CCTGCTCCCA GGGCTGTCAA
  GAGGGTTGGC TGAGATTATT TTAATTTAGT GAGATGGTGT GTGTGTGTGT GTGTGTGTGT
  A
  TGTATGTATG TGTGTTGTGT GTTTGTGTGT TCTGTGTGTG TGTGTTTACA AGCAATTGAT
  CACATTACAT TTGTAAAATG AAATACATCT TTTACATTTT T                    
  
  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	A/J
ss147557073	ENSMUSSNP4768881	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	A/J
rs108466112					SNP	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:128160650 () rs orientation: forward

Symbol	Name	Function Class
Morrbid	myeloid RNA regulator of BCL2L11 induced cell death	within coordinates
Rr564705	regulatory region 564705	76 bp distal
Rr564706	regulatory region 564706	178 bp proximal
Tssr643	transcription start site region 643	481 bp upstream
Tssr26157	transcription start site region 26157	149 bp downstream