rs46595633 SNP Detail

Summary

• ID
  rs46595633
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr1:159442275 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AAAGAAAGAA AGAAAGAAAG AGAGTCCTAT TTCCATTAAA
  CATTTATCAA ATGCTTATAG CCAAAAAAGC AAAACAACAA CAAAACCCTA GAGACTTGGG
  R
  GTGGGGGTGC AGGCATAAAC ATCCGCGCCA TTGTTCCCAT CTTGAGACAC TCACAATCTA
  GTTAGGGATG GTGACAGCTG AGCCAGAGCT GTGCAGCGA                       
  
  R = A/G
  

  
  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	A/J	DBA/2J
ss145869401	ENSMUSSNP3508605	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	G	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs46595633					SNP	G	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:159442275 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm10530	predicted gene 10530			44 bp upstream
Rr421549	regulatory region 421549			within coordinates
Rr421550	regulatory region 421550			55 bp proximal
Tnr	tenascin R			Intron
				mRNA-UTR