rs48518387 SNP Detail

Summary

• ID
  rs48518387
• 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
  

Genome Location and Flanking Sequence

• Location
  Chr12:30528382 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CAGATAAGCA TGCTTATAGC
  ATAAGCACTC GGGAGGTATA GGTAGGAGGA TTGCTGGGAG CTCGAGGCTG CTGTGTGCTC
  AATAATGGAA CCATGACTTT AAATGTGCCT TCCAAAGACA AAAGAAACTT CAACAGCTCT
  ACGACAGTGC TCCCCTGTCT CATAGTCAGT CTCCATTGTC TTGATGTGTA TTCGGCAGAC
  R
  GCTTCCTCCT AAGGCAACCA GAAGCAACAA GTAAGCCATG GTGTGAATAT GATAATAATT
  TTGCACACAA TATGGCTGAA TGAGGGTGTG ACACACTGGA TGAGGCAGAA CCTGCTCTGT
  GAATCTATGT AAATACCTGT ACATATACCT GTGAAGTTCC TATGTCCATC CCTAACTCTC
  AGAGGTGTTC GCTCCGGTAA                                            
  
  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	CAST/EiJ	MOLF/EiJ	PWD/PhJ	WSB/EiJ
ss52363837	NES15389142	PERLEGEN	MM_PANEL2	f	SNP	G	A	G	G	A
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	CAST/EiJ	MOLF/EiJ	PWD/PhJ	WSB/EiJ
rs48518387					SNP	G	A	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
ss52363837	NES15389142	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:30528382 () rs orientation: forward

Symbol	Name	Function Class
Gm28806	predicted gene 28806	819 bp downstream
Tssr113087	transcription start site region 113087	680 bp upstream