rs29644472 SNP Detail

Summary

• ID
  rs29644472
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr9:35221178 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        CAGCC TCATGATCTA ACTCATAACT
  M
  CGTTCAGTTA ACGTAGTGAG ATTGA                                      
  
  M = A/C
  

  
  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	C57BL/6J	CAST/EiJ	DBA/2J	LG/J	NOD/ShiLtJ	SM/J	WSB/EiJ
ss46325277	mCV25031150	ABI	CRAMUS_MOUSE	f	SNP	A	A		C		A
ss61379259	NES16758999	PERLEGEN	MM_PANEL2	f	SNP		A	A		A			A		C
ss136294339	ENSMUSSNP1881309	ENSEMBL	ENSEMBL_Sanger	f	SNP		A				A
ss322899713	CHEV_9_35117467	CHEVERUD	SCREENING_POP	f	SNP							C		A
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	A/J	AKR/J	C57BL/6J	CAST/EiJ	DBA/2J	LG/J	NOD/ShiLtJ	SM/J	WSB/EiJ
rs29644472					SNP	A	A	A	C	A	A	C	A	A	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
ss61379259	NES16758999	PERLEGEN	MM_PANEL	f	SNP	A/C