rs29952786 SNP Detail

Summary

• ID
  rs29952786
• Variation Type
  SNP
• Alleles
  C/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
  Chr3:36666656 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TATTAGTGAT GGGAAATAGG GGACTTCCGC TGAAATAACA
  TACCTGCTGA CATCCTAAGA TTCCAGTGAA ACTGACCATG ACTATTTACA AAAGGCACAG
  S
  GAGGAAAAAC AGCATGACTT GTTCATCAAA GGTGACTGTC ACCAGAACTT AAAAACAACC
  AATCATGAGA AAACCTGCTT GGTGCATGTA TAACTATTC                       
  
  S = C/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	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	LG/J	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
ss46899222	NES10812930	PERLEGEN	MM_PANEL2	f	SNP	G	G	C	C	G	G	C	G	C	C		C	G	G	C		G
ss134784782	ENSMUSSNP5355986	ENSEMBL	ENSEMBL_Sanger	f	SNP		G						G
ss320703499	CHEV_3_36511429	CHEVERUD	SCREENING_POP	f	SNP											C					G
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	LG/J	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
rs29952786					SNP	G	G	C	C	G	G	C	G	C	C	C	C	G	G	C	G	G

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
ss46899222	NES10812930	PERLEGEN	MM_PANEL	f	SNP	C/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:36666656 () rs orientation: forward

Symbol	Name	Function Class
Bbs7	Bardet-Biedl syndrome 7	Intron
Cpgi13088	CpG island 13088	589 bp proximal
Rr575383	regulatory region 575383	114 bp proximal
Rr575384	regulatory region 575384	768 bp proximal
Rr575385	regulatory region 575385	921 bp proximal
Tssr28874	transcription start site region 28874	975 bp upstream
Tssr33039	transcription start site region 33039	832 bp downstream
Tssr33040	transcription start site region 33040	863 bp downstream
Tssr33041	transcription start site region 33041	911 bp downstream
Tssr33042	transcription start site region 33042	954 bp downstream
Tssr33043	transcription start site region 33043	982 bp downstream