rs50806462 SNP Detail

Summary

• ID
  rs50806462
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr3:53498358 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C GAATGAAAAT CTACACAGGG AGAAGCAATC GGGGAAGAGG
  CACAGGGTCT GTTTCCTCTG AAATATTTAG AAGTAAAAAC TACAGACAAT TTATGCTGTC
  R
  GAGGCTCGCT GAGAATCAAA GGCAACAGAT CATGCGGCTG AAGCTGTGAA GGGATTGCTT
  CCTCATCGTT TGACATTTAA CTCACCTCAG CCTCTTCAAA A                    
  
  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	MSM/Ms
ss135182469	ENSMUSSNP2364455	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	G	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	MSM/Ms
rs50806462					SNP	G	G	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:53498358 () rs orientation: forward

Symbol	Name	Function Class
Frem2	Fras1 related extracellular matrix protein 2	Intron
Rr576723	regulatory region 576723	111 bp distal
Rr576724	regulatory region 576724	668 bp distal