rs107758924 SNP Detail

Summary

• ID
  rs107758924
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr12:24351475 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G CTATTCCGGA GAGTTTGCCC TTTCCTGCAC ATCATCACCT
  GCAGCTGGTT CCAAGCTCCA AGGATGAATT GGTGGGAATG GGCCTCCCCG CCTTCCTGCC
  C
  TTTATAAGTG CATTTGTCAT TAAACATTTG AACCCTGATC AGAACATTGT CTTGGCTCCG
  TTTCTCTCTC GTCCTCCTAG TTTCCCTTTC TTTAAGTGCC A                    
  
  C = C
  

  
  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
ss137381892	ENSMUSSNP5450070	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs107758924					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:24351475 () rs orientation: forward

Symbol	Name	Function Class
D12Mit282b	DNA segment, Chr 12, Massachusetts Institute of Technology 282b	1486 bp proximal
Gm4120	predicted gene 4120	1333 bp downstream