rs235380768 SNP Detail

Summary

• ID
  rs235380768
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr12:17729895 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCAAGGTTCC TGTCCTATTT
  GAGTTCATGT CCTGACTTCC CTCACTGATG GACCATGATG TGGAAGTGAA GCCAAAACAA
  ACTCTTCCTC TTCAAGTTGC TGTTGGTCAC GGTGTTTCAT CACAGCAACA GAAACCCTGA
  CTAAGACATG CTGCAAGGAA CTTGCCCATG GAGCCATCTC TCCAACCTTG AAAAGCACCC
  R
  TTTTTAAGTG TCTAGTTTAA TGAAGTTTGA CTGATGCTTA TGCCCATTTA ACCAGTGTCT
  CAGGATACAG AATGTCTCCA TCATGCCCCA AATTTCCTAG CATCCTTTGC AGTCAGTCAT
  TCACTACTCC CAACACACTT ATCAGCCCTA GATAACAACC ATCAGCCTAC TTCCTGTCTT
  ACAGAGTCAT TTCAACCTGA                                            
  
  R = A/G
  

  
  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
ss323926897	CHEV_12_17686700	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs235380768					SNP	A	G