rs46726316 SNP Detail

Summary

• ID
  rs46726316
• 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
  Chr11:73135484 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCTCCTTCCT AGCTCACTGA
  GAGGTGGAGA GACTGCCCTG AGAGCCTCGC TTCCTTGGCC TCAGTTCCTC TCTGACCCAA
  CCCTGGGTTT TGTCCTTTAA GTCTGAGGTC CTGAAAGGTT GAGCATTTGA GCACTGAAGT
  TCCTGAGTAC TGGGACTCAG AACCGGGGAG ACAGCCACCT TAGGGCTGGG TGTCTGCAGA
  C
  CATGGAGTGT GAAAGCCCCA ATTCCATTTG CTGGCCTGCA CAGTTTGGCT CACCGGCTTA
  TTCATTACAA ATTTGTTTCT TAGGCCTGTG CCCTTGAATA CTTCTGTGCT AGGCTGGGCG
  CCACCTCTCA GCTCAGCTGA GGGTGAGATG TTTTATCCTC CTCTGAGCTA TGGACTCTAT
  TAAGTTTCCA AGCTGAGTCC                                            
  
  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
ss132423148	ENSMUSSNP2218545	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs46726316					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr11:73135484 () rs orientation: forward

Symbol	Name	Function Class
Trpv1	transient receptor potential cation channel, subfamily V, member 1	within coordinates