rs31587347 SNP Detail

Summary

• ID
  rs31587347
• 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 | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr8:62403397 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCTTTATCAC GTGGCTTATT
  AGCTTAACCA TGGTGTTCCT GAAATACTGA ATCATGCCAC GCGCCAACTG CTGCAAAGCT
  AGAAGCTTCC TTTCGCCTTT TTCTCAAGCA TGTTTAAGTG CAGCCTGGTT CCTGACACAG
  AAGTAAAGAA TGTGAGGCTA CAGAATTCCC ACATAAAAGA GCTTGCTTAC ACTTTGTACT
  R
  CTGAAAACTG AGTGTATGGT CTCCCAGCCT GTCGTTCTTG GCTCACCATT TTATTTCTTT
  CAGAAAACAG ATAATTGCTT AACCCTGAAG GACATGGAAG ACTTTTGTAA GCTACATTGC
  CTCAGTGTGG CTCTTTTGCT CCATGTACCT CTCTCTCAGA GAGCTCGCTC AAGATTCATC
  ACTGCTAATT GGATTCAGGA                                            
  
  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	129S1/SvImJ	A/J	CAST/EiJ	DBA/2J	FVB/NJ	NOD/ShiLtJ	WSB/EiJ
ss47568260	NES11444592	PERLEGEN	MM_PANEL2	f	SNP	G	G	A	G	G	G	G
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	A/J	CAST/EiJ	DBA/2J	FVB/NJ	NOD/ShiLtJ	WSB/EiJ
rs31587347					SNP	G	G	A	G	G	G	G

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
ss47568260	NES11444592	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr8:62403397 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Ddx60	DExD/H box helicase 60			Intron
				Noncoding-Transcript-Variant
Tssr77513	transcription start site region 77513			1457 bp upstream
Tssr77514	transcription start site region 77514			1647 bp upstream