rs46663373 SNP Detail

Summary

• ID
  rs46663373
• Variation Type
  SNP
• Alleles
  A/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
  Chr9:52857038 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GAAACCCTGA CTAAGACACC
  TACCAAGACC AGAAACCTAC AAGTTTTGAA ACCATCCAAA AAGACACATG ACATTGGTCC
  TTTCCAGGGA TTCTTAACCC TGAAACCCAT CAACTTTCAA AGTATTTGTA AGAGAATTGT
  ATGATTTCAA TAGAAAAATA AAACACCTTT ATTTTCATAT TAAAATTTCT TATTGTGTAG
  M
  ATGTAGAAAA CAAATGACTG AAGTTAGAGG AACCTCTGCC TTTGCCTACA GAATACATCA
  TAGCTGTTTC ATGCCGTATC ATAGCTGTTT CATGCCATAT CATAGCTGTT TCATGCCATA
  TCATAGCTGT TTCATGCCAT ATCAAGGTGC TGCAGATACC TTGAGACCAT GCCTGTGCTC
  ATGGTTACTG TTTTGCAATT                                            
  
  M = A/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	CAST/EiJ	DBA/2J	FVB/NJ	NZW/LacJ	PWD/PhJ
ss61397870	NES16782945	PERLEGEN	MM_PANEL2	f	SNP	A	C	C	C	C
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	DBA/2J	FVB/NJ	NZW/LacJ	PWD/PhJ
rs46663373					SNP	A	C	C	C	C

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss61397870	NES16782945	PERLEGEN	MM_PANEL	f	SNP	A/C