rs107609067 SNP Detail

Summary

• ID
  rs107609067
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr13:50499719 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      G CCTCAGGCCA GCCTTTTTTT AATTTTTATT TTTATTAACA
  ACAGGGAGGA GATGTAGTCT CCCCTCCCCC AGCCTAAAAC CTGCTTGCTC AGGGGTGGAG
  Y
  TTCCCGCTCA ATCATTCTGC CACGCCCACT GCTAGAACAT GCCGCTTTGC TGTTTGGAGC
  CACACACTTG ATCACCCTGC TACTGGACTC CAAGATTATT T                    
  
  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	DBA/2J
ss147714015	ENSMUSSNP3483351	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs107609067					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr13:50499719 () rs orientation: reverse

Symbol	Name	Function Class
Gm8739	predicted gene 8739	1522 bp upstream