rs52611762 SNP Detail

Summary

• ID
  rs52611762
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr12:45606038 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGATTTACAA ATAATTGCAG
  AATAAAGTGA CTTTAAAATA GCTCAGATTA CATTGTAGAT CTATTTGTTA TCTCCTTTTC
  TCAGGGGGCT CAGGGAAATA TGGCAGAGAA GGGCATGTGT ATATATCAGT AGGGAAAGCA
  GAAACTTTGG CCAGATTTCA ACCATCTGTA GGAAAGAAAT ATAGCACAGA AATGAAGATT
  R
  AAAAGAACTA TTTTATTATT ATTGCCATTG TTGTTTTGTT ATTATTGTGC TTATGCATGC
  ATGGTTGCGT GTATGTATAT GTGTGTGTGT GCATGTGTAT GTGTGTTTAT GTGTGAGTTT
  ATGTGTGTGA GTGTGTGAGT TTATGTGTGT GTATATGCAT GTGTATGCCT GTGAGTGTGT
  ATGTGTCTAT GTGTGTGCAT                                            
  
  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	A/J	CAST/EiJ	KK/HlJ	MOLF/EiJ	NZW/LacJ	WSB/EiJ
ss52410613	NES15387181	PERLEGEN	MM_PANEL2	f	SNP	A	A	G	A	G	A
SNP Consensus Information
SNP					Consensus Type	A/J	CAST/EiJ	KK/HlJ	MOLF/EiJ	NZW/LacJ	WSB/EiJ
rs52611762					SNP	A	A	G	A	G	A

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
ss52410613	NES15387181	PERLEGEN	MM_PANEL	f	SNP	A/G