rs107615664 SNP Detail

Summary

• ID
  rs107615664
• Variation Type
  SNP
• Alleles
  A/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
  Chr2:50594118 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T ATGTAGTTTT ACAATTTATA TATATAGTTT ATGTACATGT
  ATATATACAC ACATATATGT ATATACATGT ATGTATGTAT ATATATGTAT ATATATATAT
  R
  TATATATATA TATATATATA TATATATATA TATATATATG GAGAGAGATA CATTGGGTTG
  TACTGAGAAT AAATAATACT TAACAAATAT ATCAAATTTA C                    
  
  R = A/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	129X1/SvJ	A/J
ss146534166	ENSMUSSNP6373720	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs107615664					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:50594118 () rs orientation: forward

Symbol	Name	Function Class
Rr556762	regulatory region 556762	722 bp distal
Rr556763	regulatory region 556763	238 bp proximal