rs27358045 SNP Detail

Summary

• ID
  rs27358045
• Variation Type
  SNP
• Alleles
  C/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
  Chr2:101865117 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GTGACCCTTC TGAACCTAAG
  CACCCCAATG TGTAAAGAGA AGGCAAGTTA TATGGACGGC TATGAGTCAG ACAAGGCGCA
  AGTGGGCGAC CTAATTAAGA AGCCAGCGTG GTGACTCAGA TGTGGTTAGA AGTCGAGGCA
  CCGTCACCAA TTTATTATCT CAATGCTGCT GTTGCTACTG CTACTTCTGA TGTGAGGCCA
  Y
  AGAGCACGTC CGAAGCCTAA GCATCTCCAG GCAAACGGGG ACGTGGCCTG AGTTTATGGC
  ATAATAAGGC ATCTAAGGCA TCTGGCCTTA TGCTTTTTCT TTTCTTTCTT TTTTTTTTTT
  TTTTTTTTTT TGGTTTTTTG AAACAGGGTT TCTCTGTATA GCCCTGGCTG GCTGTCCTGA
  AACTCACTTT GTAGACCAAG                                            
  
  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	LG/J	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
ss37579665	NES09066128	PERLEGEN	MM_PANEL2	f	SNP	T	C	T	T	T	T	C	T	T		C	T	T	C		T
ss147097697	ENSMUSSNP4817225	ENSEMBL	ENSEMBL_Sanger	f	SNP		C
ss320433798	CHEV_2_101874929	CHEVERUD	SCREENING_POP	f	SNP										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	LG/J	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
rs27358045					SNP	T	C	T	T	T	T	C	T	T	C	C	T	T	C	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
ss37579665	NES09066128	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:101865117 () rs orientation: forward

Symbol	Name	Function Class
Ldlrad3	low density lipoprotein receptor class A domain containing 3	Intron
Rr561613	regulatory region 561613	741 bp distal
Rr561614	regulatory region 561614	within coordinates
Rr561615	regulatory region 561615	1649 bp proximal