rs46187536 SNP Detail

Summary

• ID
  rs46187536
• 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 | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:121617030 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      A GATAGTCTCC AAAACACACA TTCATTTCAG TACTACTCAA
  AATATATCAC TTCCGTTTTA AAATAAATCT GAAAAAAAGA AGTGGAGGGG CTGGAGAGAG
  A
  GCTCAGTAGT ATTAACCCTG CTATCATGAA GACTGGAGTT CAGACCCCAC ACCTAGCAAA
  AGTCTGTAAC TCCAGCTCCT AGTTCGGTGG AAACAGGGTG 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	129X1/SvJ	DBA/2J
ss147399657	ENSMUSSNP6566400	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs46187536					SNP	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:121617030 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Frmd5	FERM domain containing 5			Intron
				Noncoding-Transcript-Variant
Rr563873	regulatory region 563873			785 bp proximal
Rr563874	regulatory region 563874			1277 bp proximal