rs108909901 SNP Detail

Summary

• ID
  rs108909901
• 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
  Chr10:129954133 (GRCm39)
• SNP Orientation to the Genome
  reverse

• SNP Reference Flanking Sequence

                      T AAAAACTGCC TGGTACTGGG ATAGCAACAG ACAGGTAGAC
  CAATGGAATA GAACTAAAGA CCTAGAAATG AACCCAAACA CCTATGGCCA CTGGATCTTT
  G
  ACATTGGAGC TAAAACGATC CAGTGGAAAA AAGACAGCAT TTTCAACAAA TGGTGCTGGC
  ACAACTGGCT CTTATCATGT AGAAAAATGC GAATTGATCC 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	129X1/SvJ	DBA/2J
ss144897338	ENSMUSSNP5421780	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs108909901					SNP	G	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:129954133 () rs orientation: reverse

Symbol	Name	Function Class
Gm5181	predicted gene 5181	1975 bp upstream
Rr385500	regulatory region 385500	111 bp downstream