rs27264359 SNP Detail

Summary

• ID
  rs27264359
• 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
  Chr2:143820961 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TTTCTCCACC AGCAGGGAGC GCATCAGCTC ACTCCAGGAC
  TTGCCCTGTG AGTACCTACA GACAGCTAGA GGCTAAATGG AGGTGAGAGT ATTACTATAG
  R
  TTCCCAAACA GCTCTGCCTA GGACAGACCC AGCTTATTTT CTTGCTTCTA AACAGTGTAT
  GCACTGAGAA GTCTGCAGAA TGCTAGGCTT GGAGAGGTA                       
  
  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	A/J	AKR/J	BALB/cByJ	C3H/HeJ	CAST/EiJ	FVB/NJ	MOLF/EiJ	NOD/ShiLtJ	WSB/EiJ
ss37482897	NES08934559	PERLEGEN	MM_PANEL2	f	SNP	A	A	A	A	G	A	G	A	A
SNP Consensus Information
SNP					Consensus Type	A/J	AKR/J	BALB/cByJ	C3H/HeJ	CAST/EiJ	FVB/NJ	MOLF/EiJ	NOD/ShiLtJ	WSB/EiJ
rs27264359					SNP	A	A	A	A	G	A	G	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
ss37482897	NES08934559	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:143820961 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr566349	regulatory region 566349			1724 bp proximal
Rr566350	regulatory region 566350			1931 bp proximal
Rrbp1	ribosome binding protein 1			Intron
				Noncoding-Transcript-Variant