rs27264350 SNP Detail

Summary

• ID
  rs27264350
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr2:143822428 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ACACATCACA ACAGTTATTA AGACAACTAT GGAAAGCAAG
  CTCCCTGCTT GGGCTTTCAG GCAGAGGGGC TGAAGACCAA CGAGACAGTT TCAGCAGCAG
  Y
  CAAGATTTTC GTTAGAGCCC ACAGAGAAAG ACCATGGCTT TATCATGGGC TTGACCACAG
  AAGCCTGGAC AGTAACTGAA GACCCAGCAC TGCCACAGCC                      
  
  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	C3H/HeJ	CAST/EiJ	KK/HlJ	NOD/ShiLtJ	NZW/LacJ	WSB/EiJ
ss37482888	NES08934570	PERLEGEN	MM_PANEL2	f	SNP	C	T	T	T	C	C	T	C	T
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	A/J	AKR/J	C3H/HeJ	CAST/EiJ	KK/HlJ	NOD/ShiLtJ	NZW/LacJ	WSB/EiJ
rs27264350					SNP	C	T	T	T	C	C	T	C	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
ss37482888	NES08934570	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:143822428 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr373991	regulatory region 373991			1459 bp upstream
Rr566349	regulatory region 566349			257 bp proximal
Rr566350	regulatory region 566350			464 bp proximal
Rr566351	regulatory region 566351			1684 bp proximal
Rrbp1	ribosome binding protein 1			Intron
				Noncoding-Transcript-Variant