rs31076499 SNP Detail

Summary

• ID
  rs31076499
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr18:14201937 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCTAAGCTTG CTCCTCTGGC
  TTTTGAATCT CTTATAGCAA AGAGTTAGAA CTCCAAGCCT ACCTATGTGA TTTATAATAG
  TCCTTGGATA GTCCCAGTCA TGGAGGTGGA AAGAACACAC TAAATGCCAA GGTTTTAAAG
  ACAGTGTCTC ACAGAAATGA CTATAAATAG CAGCTCAGGA GGCCACTTAC ACGAAGTTAG
  R
  CCCATTTTAG ACTAGTGGCT ATCACAGTGT AAGCTCATCA TAACTTGATT CAAGTTCAAT
  GAGCGGGAAG TAAGGATGAC CAGCCAGTGT GAGAAAGCTA GGTGGAGATC AGATAACCAC
  ATTAAAAAGA TTAAAATGCT CAGCCAGCTA TAAATGCCTG CTAAACTCCT AAAAAGGAGT
  CTGAAGAGAC CCATAAAATT                                            
  
  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	C3H/HeJ	FVB/NJ	PWD/PhJ
ss49201235	NES12682570	PERLEGEN	MM_PANEL2	f	SNP	G	G	A
SNP Consensus Information
SNP					Consensus Type	C3H/HeJ	FVB/NJ	PWD/PhJ
rs31076499					SNP	G	G	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
ss49201235	NES12682570	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr18:14201937 () rs orientation: forward

Symbol	Name	Function Class
AU018823	expressed sequence AU018823	497 bp proximal
Gm58621	predicted gene, 58621	within coordinates
Rr356066	regulatory region 356066	1569 bp distal