rs51761128 SNP Detail

Summary

• ID
  rs51761128
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:143822168 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CAATGACGAA CAGCTACATC TGAGCCCTAA ATGGTCACAG
  ACACATGTGG GGTTTCCAGT GCCCTGGCAG CAAGCACAGA AGCTGTGGAG AGTTTATTAC
  R
  GCTTTCCCCT TGGATGGAGG AAAGAATACT CTATAACCAA ACTGGGAATA TATGTGTATT
  AAATGGTACC CTACAGACTA AATGACTATT TTCCTCTTT                       
  
  R = A/G
  

  
  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
ss147776958	ENSMUSSNP3642068	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs51761128					SNP	A	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:143822168 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr373991	regulatory region 373991			1719 bp upstream
Rr566349	regulatory region 566349			517 bp proximal
Rr566350	regulatory region 566350			724 bp proximal
Rr566351	regulatory region 566351			1944 bp proximal
Rrbp1	ribosome binding protein 1			Intron
				Noncoding-Transcript-Variant