rs27517068 SNP Detail

Summary

• ID
  rs27517068
• Variation Type
  SNP
• Alleles
  G/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
  Chr4:119974676 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGTCATATGC CATAGCACCA
  AAGTCAGAGC TGGCTCCCTG TCAGACATCT CCATTCACAG CTGCCTAGGA GCTCTGAGCA
  TGATGCTAGC CTCATTGCCA CTTTGACTAG AGGACTGAAG TCCTGACTAG GGCTGGCCTG
  CCTGAGAGGC TTTCTTTGCT TTGGAGTCTC CAGGCTCAGA GCTACAGTGG AATTCAAAAA
  K
  AGTTGCCCAA GGCATGCTTG GCAGCTGTGT GTATAAACAC ATGCAAGCGC GCTCGGGCAC
  ACACACACAC ACACACACAC ACACACACAC ACCACCCAAA CCCAGACCAA AAGACAAAGA
  GCTACTTCCT ATCCCCACAG GACGTGGGAG CTCCAGAACT GGGGCTGCTG GGGCTGCTGG
  GGCTGCTGGG GCTGCTGGGG                                            
  
  K = G/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
ss37713996	NES09199660	PERLEGEN	MM_PANEL2	f	SNP	T	T	T	T	T	T	G	T	T	T	T	T	T	T	T
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
rs27517068					SNP	T	T	T	T	T	T	G	T	T	T	T	T	T	T	T

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
ss37713996	NES09199660	PERLEGEN	MM_PANEL	f	SNP	G/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:119974676 () 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
Rr598729	regulatory region 598729			1683 bp proximal