rs45849357 SNP Detail

Summary

• ID
  rs45849357
• Variation Type
  SNP
• Alleles
  A

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

Genome Location and Flanking Sequence

• Location
  Chr3:109485444 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GTCATGGCCC AGAAATACTT
  GAGTTACAGT TTTTACCTAT CTGCTTAAGG CTGTTATTCA TATTTCGTTG CTGGGAATAT
  TTTTAAATCA TGAATGAAGT TGGCCTTCCT ATACTCTATA GTCATATGAC TTTAAGAATT
  ATTAGGGTAT GACACATAAT TAGGCAAACA AAAATATTTG TGTTCATTTC AATGACTTAT
  A
  AAATGTAATG ATATTCTAAT AGAAACTTAG AGGAATCATA TTAAATTATA AATAGAAACA
  CTCAAACCAC ATTTTATTTA TGGTTAGCCA TGATTCTAAT GGGAACTAAG GCAACACTGA
  TTGTCAGAGC CTCCCTGCTG CCATGATCCT GTATCACCAA CGTGCCTGTC TTGCTTTGTT
  TTTCTTACAG AAACGGACCA                                            
  
  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	LG/J	SM/J
ss320870015	CHEV_3_109381046	CHEVERUD	SCREENING_POP	f	SNP	A	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs45849357					SNP	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:109485444 () rs orientation: forward

Symbol	Name	Function Class
Rr583434	regulatory region 583434	74 bp proximal
Vav3	vav 3 oncogene	Intron