rs234063075 SNP Detail

Summary

• ID
  rs234063075
• Variation Type
  SNP
• Alleles
  C

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

Genome Location and Flanking Sequence

• Location
  Chr3:109485131 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATGGGGGCTT CTCTGACGAA
  ACCATGTCCC TGTACCCACA AAGACAAATT CCAACACACA TAAAAAGAAA GTTCCTCTTA
  GGAAAATCTC AATAATTCAA TGGTCCCACA TACAACTTCA CATCTACTTG TATAACAAAA
  ATTAAAAAAG AAATAAATCC TTCATTAGTT CTGAGATTAC TGCAGTAGTT AAGTAACAAA
  C
  AATTCAATGC AATTCATCTA TAATCAAAAC ACATTATCAG TTAAATGTTT TCTGGAGCCA
  GAGCTCTGGG CCTTTGGTTT GAGGTTCTAT ACCTTTTTTC AGTCATTGGT CTGTCATGGC
  CCAGAAATAC TTGAGTTACA GTTTTTACCT ATCTGCTTAA GGCTGTTATT CATATTTCGT
  TGCTGGGAAT ATTTTTAAAT                                            
  
  C = 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	LG/J	SM/J
ss320870013	CHEV_3_109380733	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs234063075					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:109485131 () rs orientation: forward

Symbol	Name	Function Class
Rr583434	regulatory region 583434	387 bp proximal
Vav3	vav 3 oncogene	Intron