rs45847352 SNP Detail

Summary

• ID
  rs45847352
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:191710672 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACTCACTAAT CCAACCACCC
  ACCCACTCCC TGATCCAACC ACCCCTTGAT CCAACCAACC CCTGATCCAC CCATTCACTG
  AACCACCCAC CCACCCACCA CTGATCCACC TATCCACTCA TATCCCCACT TGCCCAGGCA
  TTCATTCGCC CATCATTACA CATGCTGGGA TGATGGAGCT GATGGCCTCT GAGATCCATG
  Y
  CATCTCTGTG GGGAACATGA GGGCCAGGCT ACAGGAAGAA GTTGACTCTT AGACACTGGT
  TTGAGGGATG AGCAGGTCTT TGTCAGGTAG GTAAAAGACC CACAGGTCGG GCAGGTTTAC
  ACCTGGCTTG GTGGTGTAGA GATAATTTTT TTAATGCCAA AAAGAAACAA GGAGAACTTG
  CAGCTTGTGA CGTTGACTTT                                            
  
  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	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
ss60361404	NES15865093	PERLEGEN	MM_PANEL2	f	SNP	C	C	C	C	C	C	T	C	C	C	C	C	C	C	C
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
rs45847352					SNP	C	C	C	C	C	C	T	C	C	C	C	C	C	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
ss60361404	NES15865093	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:191710672 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm70534	predicted gene, 70534			527 bp upstream
Rd3	retinal degeneration 3			Intron
				mRNA-UTR
Rr426276	regulatory region 426276			1328 bp distal
Rr426277	regulatory region 426277			1146 bp distal
Rr426278	regulatory region 426278			576 bp proximal
Tssr10797	transcription start site region 10797			1322 bp downstream
Tssr10798	transcription start site region 10798			1311 bp downstream
Tssr10799	transcription start site region 10799			1266 bp downstream
Tssr10800	transcription start site region 10800			452 bp downstream
Tssr10801	transcription start site region 10801			420 bp downstream