rs107943054 SNP Detail

Summary

• ID
  rs107943054
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr1:160902297 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TGGTTGCTGG GATTTGAATC AGGACCTCTG GCAGAGCAGT
  CAGTGCTCTT AACTGCCCAG CCGTCTCTCC AGTCCCCTGA CTTTTTAGTG ATTAGAGTTC
  Y
  AGTTACCTTT TTTTTTTTTT TAAATGCAGA CCATGGATTC CTGTGATTTT CGAGGACTGA
  CTTCTAGACG AAGGACCTCA AATCTTAAGA ACTACTTTG                       
  
  Y = C/T
  

  
  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	DBA/2J
ss145905431	ENSMUSSNP609137	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs107943054					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:160902297 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cenpl	centromere protein L			Intron
				Noncoding-Transcript-Variant
Rr396459	regulatory region 396459			1560 bp upstream
Rr421753	regulatory region 421753			1982 bp distal
Rr421754	regulatory region 421754			1507 bp proximal