rs29716298 SNP Detail

Summary

• ID
  rs29716298
• 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
  

Genome Location and Flanking Sequence

• Location
  Chr3:14454589 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GCTCATGGCA GCTCCTTGTA GAAAAGGATA GTGTCTGGGA
  CCCTGAGAAG CAGGAGACAC ATTCCTCCAG GGGACCCACC ATCTGAAATA AAGGACTGCC
  Y
  GCAGTAGGCC AGGATAGAGA CATCTCAGTA GCCCTCGGCA GCTCTTTGTA AAAAAAGTTA
  TTCCCAGTTC TCCTAACCTT AGCCCTGGAC AACGACTGTA                      
  
  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	DBA/2J	FVB/NJ	NOD/ShiLtJ	NZW/LacJ	WSB/EiJ
ss49561564	NES12895764	PERLEGEN	MM_PANEL2	f	SNP	T	C	T	C	T	C	T	T	C	C	T
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	DBA/2J	FVB/NJ	NOD/ShiLtJ	NZW/LacJ	WSB/EiJ
rs29716298					SNP	T	C	T	C	T	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
ss49561564	NES12895764	PERLEGEN	MM_PANEL	f	SNP	C/T