rs29650734 SNP Detail

Summary

• ID
  rs29650734
• Variation Type
  SNP
• Alleles
  G/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
  Chr3:28475279 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CAGGTAAAGG GTGGTTTAAG TATGGTCTTA ATTCTTTTGA
  GACAACCATC CCTCCTCTCT CTCTCTCTCT CTCCTCTCCC TTTTTTCCCT TTAATGTGAT
  K
  TATTTATTTT TATTTCATGT GTATGGCTGT TTTACCTGCA TACATGTCTG TGCATCATTT
  GTGTGCTAGG TGACTGTGGG TGGGAGTCAG TCTCAGTCTA                      
  
  K = G/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	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	KK/HlJ	MOLF/EiJ	NZW/LacJ	WSB/EiJ
ss46869042	NES10812699	PERLEGEN	MM_PANEL2	f	SNP	G	G	T	T	T	T	T	G
SNP Consensus Information
SNP					Consensus Type	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	KK/HlJ	MOLF/EiJ	NZW/LacJ	WSB/EiJ
rs29650734					SNP	G	G	T	T	T	T	T	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
ss46869042	NES10812699	PERLEGEN	MM_PANEL	f	SNP	G/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:28475279 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Mir466q	microRNA 466q			1112 bp downstream
Rr574579	regulatory region 574579			471 bp distal
Rr574580	regulatory region 574580			974 bp proximal
Rr574581	regulatory region 574581			1245 bp proximal
Tnik	TRAF2 and NCK interacting kinase			Intron
				Noncoding-Transcript-Variant