rs108667872 SNP Detail

Summary

• ID
  rs108667872
• Variation Type
  SNP
• Alleles
  A

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr17:81772706 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CCGATTCTTT CCCCCAAAAG AATGATTTTA GGATAAAATG
  CCCACAGAAT ATGAAATCTT TTTCTTGAAT AATGTTGCTG AAAACAGTAT GCTAAAGAGG
  A
  AGGGGGGGTG GAAGGAAAGA AAGTGGTTGG AGGAAGCCCA AGTGATTGCA GAATCCTTAT
  GAACTGTGGG GTGTAGGGTC AGACATGTTT GAGCTTGAA                       
  
  A = A
  

  
  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	C57BL/6J	C57L/J	RF/J	RIIIS/J	SJL/J
ss399210585	MGP_WTSI_17_81864617	EVA_MGPV3	EVA_MGPV3	f	SNP	A	A	A	A	A
SNP Consensus Information
SNP					Consensus Type	C57BL/6J	C57L/J	RF/J	RIIIS/J	SJL/J
rs108667872					SNP	A	A	A	A	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
ss399210585	MGP_WTSI_17_81864617	SC_MOUSE_GENOMES	SC_MOUSE_GENOMES	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr17:81772706 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Slc8a1	solute carrier family 8 (sodium/calcium exchanger), member 1			Intron
				Noncoding-Transcript-Variant
Tssr149528	transcription start site region 149528			358 bp downstream