rs45906962 SNP Detail

Summary

• ID
  rs45906962
• Variation Type
  SNP
• Alleles
  A/T

• 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
  Chr10:8858964 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTGAATGTTC CCTTGGGGCT
  GGAGAGATGG CTTAGCTGTT AAGACCACAG TCTGCTCTTC CAGAGGTCCT GAGTTCAATC
  CCCAGCAACC ACATGGTGTC TCATAATCAC CTATAGTATG ATCTGGTGCT GTCTTCTGGC
  ATGTAGATGT ACATATAAAT AGAGCACCCA CATACATAAA GTAAATAAAT CTTAAAATAA
  W
  TTTGGAAAAA GTGTTCCCTT TATTTCTAGA TTTGTACCTT TTTAAAATTT TTTTTTATTC
  TGAGACAGGG TTTCTCTGTG TAGCCCTGGC TGTCCTGGAA CTCACTCTGT AGACCAGGCT
  GGCCTCAAAC TCAGAAATTC GCCTGCTGCT GCCTCCCAAG TGCTGGGATT AGAGGCATGC
  ACCACCACGC CTGGCCCGCT                                            
  
  W = A/T
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

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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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss146769184	ENSMUSSNP1426296	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	T
ss323246168	CHEV_10_8703018	CHEVERUD	SCREENING_POP	f	SNP				A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs45906962					SNP	A	A	T	A	A