rs107763912 SNP Detail

Summary

• ID
  rs107763912
• Variation Type
  SNP
• Alleles
  T

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

Genome Location and Flanking Sequence

• Location
  Chr4:147893877 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T TGGAAGGTGA CAGGACCAGC TGCTCAATGT CCTAGGAGGC
  CAGCACAGCA ATTGCAGCTT AAAGAAGTTT TCAGGTTCCG CAAACACTGA ATTGTGAGAG
  T
  GGCGGCAGAA AATGCACCCC TGCTCCACGC CCCTGCCCAG CTCCTGCCCG TTCCCCAGTC
  CAACAGCTCC TCTGACTTGG AAGGTGACAG GACCAGCTGC T                    
  
  T = 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	DBA/2J
ss147982744	ENSMUSSNP449695	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs107763912					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:147893877 () rs orientation: forward

Symbol	Name	Function Class
Gm20707	predicted gene 20707	within coordinates
Rr377386	regulatory region 377386	within coordinates
Rr604501	regulatory region 604501	608 bp distal
Rr604502	regulatory region 604502	within coordinates
Rr604503	regulatory region 604503	358 bp proximal
Tssr44548	transcription start site region 44548	382 bp downstream
Zfp984	zinc finger protein 984	Intron