rs27515986 SNP Detail

Summary

• ID
  rs27515986
• 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
  Chr4:119669172 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCCTGTGTGC ATATGTGGAG
  TATTTTTAGT GGCCTCCAAG GGAGCTGCTA CCTACCCTGC CTGCTCCTCC TCATTTTTAG
  TTCCTACTTA TATCAGGAAC AAAATTCCCA ATTTGCAAAG AAGCTCTGAA AAAGCTTCCG
  TTTCTAGCCA TTCTGTCTTT AGTGAGCTGG TCTTGCTCCC CATGACCTGA TCTGTCTCTG
  Y
  ATTTCTTTAT ACCCATAAAC GTCCTCCAGC CTCCATCTTC TGAGCCTGAA CCTTCTAGGA
  CCCTTTCCTG GGAACCTATG CAATGACTTC TTCAAGGTCT GTGCAGAATC TTCACAAACT
  TTCCTGCCCC GCACCTCACG ACTCTGAATC TTTTACTCTT TCAAATGCCT ACATCTTGAT
  GGTACAATCC TTTGGTTTCC                                            
  
  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	AKR/J	CAST/EiJ	NOD/ShiLtJ	NZW/LacJ
ss37715112	NES09198896	PERLEGEN	MM_PANEL2	f	SNP	C	T	C	C
SNP Consensus Information
SNP					Consensus Type	AKR/J	CAST/EiJ	NOD/ShiLtJ	NZW/LacJ
rs27515986					SNP	C	T	C	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
ss37715112	NES09198896	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:119669172 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Hivep3	human immunodeficiency virus type I enhancer binding protein 3			Intron
				Noncoding-Transcript-Variant
Rr398435	regulatory region 398435			867 bp upstream
Rr398436	regulatory region 398436			1425 bp upstream
Rr598655	regulatory region 598655			698 bp proximal
Tssr38753	transcription start site region 38753			1081 bp upstream