rs28267767 SNP Detail

Summary

• ID
  rs28267767
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr2:153266439 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GTGAAAGTGG CCTTCTTCTA
  CCCAACACCC CCTTCCTTCT TCCTCACCTG CTTCCTATGC TGTGTCCCCG GACTGACAAG
  CACTGCAAGG GGGGAAGGAA TCACGATCCG GCAGCGCATC TCCTGGTCCA TGCACTGCTC
  TGCCCTTCCT TCAGAGCTTC CGTGAACATC CTTTCCCCAG GGAAGGTTCC CACCGTGCCT
  R
  TCCCATCTCA TCCTGGCACA AGCTCTGGCT GCTCTTCTGC ACGACTCCTC CCAAGGAAGT
  TGGCCCTATA GCCACACGAT TGTAGCCGTG GCACCCTTCT CCCACTGGGC CACAGGGTCT
  ACTGCCCTGC TCTCCCCTTG CAGCTCAACC TGCCATCTCG CTGTGGCCTT GGCCTTCTGT
  ACTTCCGTCA CCTCTTGCTG                                            
  
  R = A/G
  

  
  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	BTBR T<+> Itpr3/J	CAST/EiJ	MOLF/EiJ	NOD/ShiLtJ	PWD/PhJ
ss37559796	NES08910636	PERLEGEN	MM_PANEL2	f	SNP	A	G	A	A	A
SNP Consensus Information
SNP					Consensus Type	BTBR T<+> Itpr3/J	CAST/EiJ	MOLF/EiJ	NOD/ShiLtJ	PWD/PhJ
rs28267767					SNP	A	G	A	A	A

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
ss37559796	NES08910636	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:153266439 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Nol4l	nucleolar protein 4-like			Intron
				Noncoding-Transcript-Variant
Rr567635	regulatory region 567635			1042 bp distal
Rr567636	regulatory region 567636			65 bp proximal
Tssr699	transcription start site region 699			174 bp downstream