rs49070174 SNP Detail

Summary

• ID
  rs49070174
• Variation Type
  SNP
• Alleles
  G/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
  Chr9:44475590 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAAGGCAGTG GGTCTGCTTT
  TATTCATTTG CATTACCTGT TAAATGGCTA AGTCACCTTT GCTTGACAGC TTTTGTAATT
  CACCAATAAG AAAGATGTGG ACTCCTCTGT CCGTCCGTCC GTCCGTCTGT CCCTTCCCAG
  CCAACCCCTG CGGTCCTCAC AGAGATGCTG CTCACCATCC TGTCTCCCAA GGCCCTGGTG
  K
  GGCTTTGAGG CATCACCATA CTGCACTGAC CCTAGCTCTC TGGTTTCTTC TTCTAATCCT
  TGAAGCTTTG GAGGACAGTA CGCTGTCTCC CAGGCTTCAG GCCTGCGCAT CTTCTCCTGA
  GTCTGGTGCA GTCTGAGATG ACTGTTCATC CTCCTTCAGT TCATCTAGGA ATCAAGGACC
  TAGGGCTGGT GACGCAGGCC                                            
  
  K = G/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	129X1/SvJ	A/J
ss136397245	ENSMUSSNP513829	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs49070174					SNP	G	T