rs46496542 SNP Detail

Summary

• ID
  rs46496542
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr13:25778453 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GATGAGTTTT TTTTTATATT CAGCAATCAA TGCTACTCAA
  AGCTTTCAGC CAGTGATTCC ACTAAGCATT AATTCATCAA ATTATCAAAA TGACTTAACA
  C
  AGTCTTAACC TAGTCATATT TATGAAAGTA AAAATTTCTC TATTAAGTCA TGTGAATTAG
  GAGGGGGGAG TGCCCTCAAT CCTTTTGGTA TCCTGAACGG C                    
  
  C = C
  

  
  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	DBA/2J	MSM/Ms
ss148814756	ENSMUSSNP4823586	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	C
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	MSM/Ms
rs46496542					SNP	C	C	C