rs252172634 SNP Detail

Summary

• ID
  rs252172634
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr12:17729843 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGGGCCAGCC AGTAAGAAAC
  ACTCTTCCGC CGCCTCTTCT TCAGTTTCTG TTTCAAGGTT CCTGTCCTAT TTGAGTTCAT
  GTCCTGACTT CCCTCACTGA TGGACCATGA TGTGGAAGTG AAGCCAAAAC AAACTCTTCC
  TCTTCAAGTT GCTGTTGGTC ACGGTGTTTC ATCACAGCAA CAGAAACCCT GACTAAGACA
  Y
  GCTGCAAGGA ACTTGCCCAT GGAGCCATCT CTCCAACCTT GAAAAGCACC CGTTTTTAAG
  TGTCTAGTTT AATGAAGTTT GACTGATGCT TATGCCCATT TAACCAGTGT CTCAGGATAC
  AGAATGTCTC CATCATGCCC CAAATTTCCT AGCATCCTTT GCAGTCAGTC ATTCACTACT
  CCCAACACAC TTATCAGCCC                                            
  
  Y = C/T
  

  
  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
ss323926895	CHEV_12_17686648	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs252172634					SNP	C	T