rs48286618 SNP Detail

Summary

• ID
  rs48286618
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:155093692 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CTAATGTTTT CAGGAGCCCT TCCCCCTCAA AGTCCTTCCA
  TGAAACCCTG AGTAAAAATG GATGACCAAG GGGGCCTGGG CCAGGAACCA AGGGTCTCTC
  Y
  GGGGGTTCTC ATCTGGGTGT TTAGAAAGAT CTTTAGCTGT GTTACTGATC CCAGGATGTC
  AGCAGACAGC CAAGGGAGAG AGGCTTCAAG CCTGCCAGC                       
  
  Y = C/T
  

  
  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	129X1/SvJ	DBA/2J
ss145777645	ENSMUSSNP3037972	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	DBA/2J
rs48286618					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:155093692 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
BC034090	cDNA sequence BC034090			Intron
				Noncoding-Transcript-Variant
Rr420975	regulatory region 420975			736 bp distal
Rr420977	regulatory region 420977			95 bp proximal
Rr420978	regulatory region 420978			432 bp proximal
Rr420979	regulatory region 420979			1088 bp proximal