rs108137186 SNP Detail

Summary

• ID
  rs108137186
• Variation Type
  SNP
• Alleles
  C

• 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
  Chr1:135238776 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CAACTGTGTT TCTGTAAGGA TTTATGTAAG CTTCTCTTTT
  GTTATCACAC AAAGCCTACA CACACACACA CACACACACA CACACACACG ATCACCCCAC
  C
  CCCTACCCCC ACAGTACAGG GTAAATTCTG TTTCAAGCAA CTCTCAGCAG AGTTGTAATT
  CTCTACCACC ATCTCCTTCC AAATAAGAAG CTGGGAGTC                       
  
  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	A/J
ss145530421	ENSMUSSNP6256491	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs108137186					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:135238776 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr419124	regulatory region 419124			340 bp proximal
Timm17a	translocase of inner mitochondrial membrane 17a			Intron
				mRNA-UTR