rs107691595 SNP Detail

Summary

• ID
  rs107691595
• Variation Type
  SNP
• Alleles
  G

• 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
  Chr13:11502764 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C TAAAAGTCTG TTTTATCAAA TGGAACTACA ACACTCATAG
  GAAATTTAGA TAGGTAGGTA GACAGACAGA CAGACAGACA GACTGACTGA CTCACTGACT
  G
  ACTGACTGAC TCACTGACTG ACTGACTGAT ATGGGACAGC CATATATTTA CAGGCCAAAA
  GAAAAAAATA AAGAAGGATG GTCAACTGGA ACTACAACCG A                    
  
  G = G
  

  
  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
ss148674835	ENSMUSSNP5926791	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs107691595					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr13:11502764 () rs orientation: forward

Symbol	Name	Function Class
D13Ertd463e	DNA segment, Chr 13, ERATO Doi 463, expressed	23 bp proximal
Rr387978	regulatory region 387978	1907 bp upstream