rs46865223 SNP Detail

Summary

• ID
  rs46865223
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:58636147 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T TGGCCCAGGG AGTGGCACTA TTAGGAGGTG TAGTCTTGTT
  GGAGTAGATG TGTCATTGTG GGTGTGGGCT TTAAGACCCT TGTTGTAGCT GCCTAGAAGT
  Y
  AGTCTTCCAC TAGCAGCCTT CAGATGAAGA TGTAGAACTC TCAGCTCCTC TTGCACCATG
  CCTGCCTGGA TGCTGCCATG TTCCTGCCTA GATGATAATG G                    
  
  Y = C/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	DBA/2J
ss146360525	ENSMUSSNP6107714	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs46865223					SNP	C	T	C