rs107876646 SNP Detail

Summary

• ID
  rs107876646
• Variation Type
  SNP
• Alleles
  G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr12:19296080 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ACCCGTCACC TTCCTGGTAG ATACTGGGGC CCAACACTCC
  GTGCTGACCC AAAATCCTGG ACCCCTAAGT GACAAGTCTG CCTGGGTCCA AGGGGCTACT
  G
  GAAGAAAGCG GTATCGCTGG ACCACGGATC GCAAAGTACA TCTGGCTACC GGTAAGGTCA
  CCCACTCTTT CCTCCATGTA CCAGACTGCC CCTATCCTC                       
  
  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
ss137247386	ENSMUSSNP6844828	ENSEMBL	ENSEMBL_Sanger	f	SNP	G
SNP Consensus Information
SNP					Consensus Type	A/J
rs107876646					SNP	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:19296080 () rs orientation: forward

Symbol	Name	Function Class
Gm40843	predicted gene, 40843	within coordinates
Gm51522	predicted gene, 51522	135 bp upstream