rs222164910 SNP Detail

Summary

• ID
  rs222164910
• Variation Type
  SNP
• Alleles
  C

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

Genome Location and Flanking Sequence

• Location
  Chr4:108188343 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    TACTCCTAA GAACCCTTTG TGCGTTATGG
  TCTGTAGTAA CATGCCCATT GTGGAGAGAG GCGCAGCTCT AATTTCTTCA TGTGTTTGAG
  GTTCTTGCCT CCCTAACCCA TACCGCCTTA TCTTGGCCTC CTTCTACCAC ATTTGTGCCG
  C
  GTTTATTTCC CCTTCCACCT GTTTCTGGAC TCTCTCCATT TCTTTGTCTT GATTCGATAG
  GGATGGAGCC ACCCAGGGCC TTGTACTTTG CCTTGTCATG CATGGAGTGA CACCTTCAAC
  TCCTTAGTCC TTATGTATCC TGTGCTCTCT                                 
  
  C = 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	LG/J	SM/J
ss321252427	CHEV_4_108003751	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs222164910					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:108188343 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Coa7	cytochrome c oxidase assembly factor 7			Intron
				Noncoding-Transcript-Variant
Rr597155	regulatory region 597155			1917 bp proximal