rs49017785 SNP Detail

Summary

• ID
  rs49017785
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:149697560 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AGAAAAGATG GTAAACAGGA CAAGGGGATG CAGACCTGTT
  TAGAAGTAGT TCTTTGGGGC AATTCCAGTC TCCATTTGTT AGGATACCAA TAGCCCAGTT
  M
  AAATGTGTCA CCAACCGCAA ACCAGCAAAA ACTGCATGAT CCAGCAGAAA CTGCCAGGAC
  TCCACCAATT TGACATGAGT CAGCAGGGGT GACCAGGAC                       
  
  M = A/C
  

  
  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
ss136076349	ENSMUSSNP5148117	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs49017785					SNP	C	C	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:149697560 () rs orientation: forward

Symbol	Name	Function Class
Gm65521	predicted gene, 65521	within coordinates
Rr587357	regulatory region 587357	1478 bp proximal