rs39161442 SNP Detail

Summary

• ID
  rs39161442
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  126
• Last Updated in dbSNP Build
  126
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr7:74276677 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GTGTTCTGGA TGTGTCCTGG GAGCTGGGGT CTTTCCCAAT
  GGGCACTCAG GACTGGTGGA AGGAGGTGGG GATGAGGCAC ATCATACTAA GTGTGTGGAG
  R
  CTGTCCCCTC ACTCTGTACA GTGGATTTCT CCTGATTGCC TCTTAAGGAT TCATTATATC
  ATTTTAAGCA ACTGCCTCCT TGCTTGCTCA TATGGTCCAT                      
  
  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	FVB/NJ	MOLF/EiJ	PWD/PhJ
ss50413555	NES13944696	PERLEGEN	MM_PANEL2	f	SNP	G	G	A
SNP Consensus Information
SNP					Consensus Type	FVB/NJ	MOLF/EiJ	PWD/PhJ
rs39161442					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
ss50413555	NES13944696	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:74276677 () rs orientation: forward

Symbol	Name	Function Class
Gm39037	predicted gene, 39037	within coordinates