rs29315785 SNP Detail

Summary

• ID
  rs29315785
• 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
  Chr10:67702488 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        ACTCG CTAAGCCTCG TAATGACTGG
  M
  GACCGAGTGC CAAATCTGGG CTTAC                                      
  
  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	129X1/SvJ	A/J	AKR/J	BALB/cByJ	C3H/HeJ	DBA/2J	KK/HlJ	LG/J	PWD/PhJ	SM/J
ss38518570	mCV24513222	ABI	CRAMUS_MOUSE	f	SNP			A				C
ss50874750	NES14165827	PERLEGEN	MM_PANEL2	f	SNP	A		A	A	A	A		A		C
ss147133253	ENSMUSSNP1581141	ENSEMBL	ENSEMBL_Sanger	f	SNP		A	A				C
ss323348836	CHEV_10_67329406	CHEVERUD	SCREENING_POP	f	SNP									A		A
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	A/J	AKR/J	BALB/cByJ	C3H/HeJ	DBA/2J	KK/HlJ	LG/J	PWD/PhJ	SM/J
rs29315785					SNP	A	A	A	A	A	A	C	A	A	C	A

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
ss50874750	NES14165827	PERLEGEN	MM_PANEL	f	SNP	A/C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:67702488 () rs orientation: forward

Symbol	Name	Function Class
Rr223271	regulatory region 223271	1626 bp proximal