rs46413298 SNP Detail

Summary

• ID
  rs46413298
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:86808312 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C TTTCTGCTTT TTGATAACTC TATGGATAGC ACTTTTCACT
  TCTTTGTTTC TGAGACTATA AATGAGTGGG TTCAGCATGG GGATCACTAT AGTATAGAAA
  C
  CAGAAGCCAC TTGTTCCTTT CCTGAGTAGT AGGAATTACT TGGTTTCAAG TAAGTAAAAA
  TCAAAGTACC ATAAAAGACA GTGACTCCTA GGAGATGAGA A                    
  
  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
ss146867518	ENSMUSSNP5295252	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs46413298					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:86808312 () rs orientation: forward

Symbol	Name	Function Class
Or8h10	olfactory receptor family 8 subfamily H member 10	Coding-NonSynonymous