rs107701746 SNP Detail

Summary

• ID
  rs107701746
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr3:61552537 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      G TTGAACATTT TTTCAGGTGC TTCTCAGCCA TTCGGTATTC
  CTCAGGTGAG AATGCATTGT TTAGCTCTGA GCCTCAATTT TTAATGGGGT TATTTGATTT
  C
  CTGGAGTCTA TCTTCTTGAG TTTCTTATAT ATATTGGATA TTAGTTCCCT ATCTGATTTA
  GGATAGGTAA AGATCCTTTC CCAATCTGTT GGTGGCCTTT T                    
  
  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	A/J
ss135291634	ENSMUSSNP3292141	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs107701746					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:61552537 () rs orientation: reverse

Symbol	Name	Function Class
Rr375072	regulatory region 375072	1564 bp downstream