rs107754058 SNP Detail

Summary

• ID
  rs107754058
• 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
  Chr4:17656593 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      A TGCTACCATG GCGAAAGTGC GGGCCACACA CTCTGCACCT
  AACACATGTG CCAAACACAA AACACACACA CACTATAACA AGCATACATC CCAGGGCTCT
  C
  ATCCCTACTC ATCTTCCCTG AAGCAAGGGA TAGATAGCCA GCGGGGCTAT CTCTTTAAGG
  GGAATTCAGG GATCAAAAAG CGTGGAAAAA TTTGAATGTC 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	129X1/SvJ	DBA/2J
ss146067471	ENSMUSSNP4153807	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs107754058					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:17656593 () rs orientation: forward

Symbol	Name	Function Class
Gm11851	predicted gene 11851	82 bp downstream