rs108907295 SNP Detail

Summary

• ID
  rs108907295
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr2:168431246 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      C GCAGCCACTG AGGCATCTGG AAGCTGCCAG CAGGCTTGCC
  CCTGAGCCTG CCGCAGGCAA GGGCTGGGCT GTCAAAATCA GGAAACCTGG TTAGGTTTTC
  Y
  TGTTTGCTCC CAGGCAACAA GTTTTCTAAC CAGAAAATGC AATGTGAAGC TGGGCATAAA
  GCCTGCTACC GCCTCTGACA GATGCTGTTA AATGCTGGAG T                    
  
  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	129X1/SvJ	A/J	DBA/2J	MSM/Ms
ss148270641	ENSMUSSNP929401	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	MSM/Ms
rs108907295					SNP	T	T	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:168431246 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cpgi12775	CpG island 12775			352 bp proximal
Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2			Intron
				Noncoding-Transcript-Variant
Rr571025	regulatory region 571025			1854 bp distal
Rr571026	regulatory region 571026			within coordinates
Rr571027	regulatory region 571027			855 bp proximal
Tssr21877	transcription start site region 21877			1115 bp upstream
Tssr27851	transcription start site region 27851			965 bp downstream
Tssr27852	transcription start site region 27852			989 bp downstream