rs108907054 SNP Detail

Summary

• ID
  rs108907054
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr8:36193380 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AACAAAAACA AAAATAAAAA GCCCAACCCA TCAACCAATC
  AACCAGCCCA CCCCCTTCTC TTTCCCTCCT CCCCTCTCAA GCAATACAAA CGTCATGGCA
  C
  GAATCCTTCG TTTTACCTTA TACTTGAATG TGTACCGTCT CTCTGAGCAT GCTCATTAAT
  CTGTCTGCCC CGCAGGACAA AGAATTACTC CCAGGCTCC                       
  
  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	A/J
ss149167697	ENSMUSSNP2698716	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs108907054					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr8:36193380 () rs orientation: forward

Symbol	Name	Function Class
Gm35021	predicted gene, 35021	within coordinates
Gm40492	predicted gene, 40492	1457 bp downstream
Rr662255	regulatory region 662255	772 bp distal
Rr662256	regulatory region 662256	633 bp distal