rs27289047 SNP Detail

Summary

• ID
  rs27289047
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:168406196 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AATGGTGTAA AGGCCCCACT
  GAGAGCTGGA GCTTCCTCCG TCTCTCTCCT GATCTCTGCC ACTGTCACAT CTACTCCTGT
  TTCTGAGGCC AAACTGCGCC CAGCTTCTCA CGCAGCTTCC CCGCCACCCT GCCACAGGCC
  TCAGCACACA GTGCTGATCC TCTAGTCAGA GTCAGTCAGA ATCCTCAGAG GGACCAGGAC
  Y
  TGGGCTCCAA TGAGCTGGCA AGAGGGTCAG AGCCAGGACA GTAGGTGACG CGGTAAAGAG
  AGAAAAGGCA GGAGGTATGG ACACCAGATT TCTCTGTGAG AGGGAAGCCA AGCTGAGCTG
  TCCACGGGCG ACGAGCAAGG TCCCCGAAGC AACTGTTACT GTCATGAAAC AGCAATGACC
  TTGAGCAAGT TTTGAGACCT                                            
  
  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	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss37504669	NES08836398	PERLEGEN	MM_PANEL2	f	SNP	C	C	C	C	C	C	T	C	C	C	C	C	C	T	C
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
rs27289047					SNP	C	C	C	C	C	C	T	C	C	C	C	C	C	T	C

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss37504669	NES08836398	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:168406196 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm74616	predicted gene, 74616			1283 bp upstream
Nfatc2	nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2			Intron
				Noncoding-Transcript-Variant
Rr571014	regulatory region 571014			350 bp distal
Rr571015	regulatory region 571015			34 bp proximal
Rr571016	regulatory region 571016			1324 bp proximal