rs46613178 SNP Detail

Summary

• ID
  rs46613178
• Variation Type
  SNP
• Alleles
  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
  Chr4:143813385 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TGCAGGGACA GACTGAACCA CCATCAGTCT TTCTTGAGCG
  TCTAATGGAG GCATATAGGA GATACACCCC TTTTGACCCT TTGTCAGAGG GGCAGAGGGC
  C
  GCTGTAGCCA TGGCCTTCAT TGGTCAGTCC GCTCCCGACA TTAAGAAAAA GCTGCAAAGG
  CTGGAGGGGC TCCAAGATCA TACGCTCCAA GATTTAGTA                       
  
  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
ss147812726	ENSMUSSNP1106039	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs46613178					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:143813385 () rs orientation: forward

Symbol	Name	Function Class
Rr604217	regulatory region 604217	1871 bp distal