rs232939363 SNP Detail

Summary

• ID
  rs232939363
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr12:26806577 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GTCTAGGCTC CACCCCCACA GTTACCTGGC AACAGCCAGG
  TATGCTCCTC CCCCCAGTTA CCTGGCAACA GCTAGGTAGC TCAATTCACT ATAAAAGGAG
  C
  TGCTTGCCCC CTCCTTGCTC TCTTGCCTTT TTTACCCTTT TATTCTCTTA CTCTTGCCTC
  TCCCCCTCCT GCTCCCCCTC CCTTCTCCAC ATGGCCATG                       
  
  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	LG/J	SM/J
ss323954145	CHEV_12_27441443	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs232939363					SNP	C	C