rs50320729 SNP Detail

Summary

• ID
  rs50320729
• 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
  Chr13:58636309 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGTGGACTTT AAGACCCTCA
  TCCTAGCTGC CTGGAAGTGA GTCTTCTACT AGTGGCCTTC AGATGAAGAT GTAGAACTCT
  CAGCTCCTCC TGCACCATGA CTACCTGGAT GCTTCCATGT TCCCACCTTG ATGATAATGG
  ACTGAACCTC TGAACCTGTA AGCCAGCCCT AATTAAATGT TGCCCTTTAT AATTCTTGCC
  W
  TGGCCATGGT ATCTGTTCAC AGCAGTAAAA CTAAGACAGG AGGTCAATGC CTGGAAAACT
  ACATCAGTCA GGGCCCGGAC CGGAGAGACC CATGGGGCTC ACAACAATCC ATTCTGCACC
  TCCAAGGTGA AGTGTGATGT TGAGGGCCAG GCAGAAGTGT GCCAGTTCTG AGAGTTCCTG
  AAGAATAAAT TATTTTATAT                                            
  
  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	MSM/Ms
ss149066706	ENSMUSSNP396069	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T	T	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	MSM/Ms
rs50320729					SNP	T	T	T	A