rs46721632 SNP Detail

Summary

• ID
  rs46721632
• 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
  Chr6:139438590 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ATATGTTGCC ACCAGTGTCT GCAGAACTTT AACGAGAAGC
  AGATATATCC CAATTATTCT ACTTAGTAGG CATCCAAAAT AAGTGTCACC AGGGCAGTAG
  M
  TGTGTGGGAA GCATGAAGAC ACTGAGTTTC TAAAGAGATC ATATTACCTT CACAACGTCC
  CGGAGGACAG TTTTATAGAC ACTGGAAATT CAAATAAAA                       
  
  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	A/J	DBA/2J	LG/J	SM/J
ss133916394	ENSMUSSNP5164261	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
ss322019571	CHEV_6_139410113	CHEVERUD	SCREENING_POP	f	SNP			C	A
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	LG/J	SM/J
rs46721632					SNP	C	C	C	A