rs30393315 SNP Detail

Summary

• ID
  rs30393315
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr3:53496639 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTACAGATCC TATTAAGTGG
  GCGTTTCTCA AAGTGACATC TCTGTGTCAT CAAGGGCTTC AGAACTCTAC ACCAACTATA
  TTTCTGCTTC ATATCTTTCC ATATTTTATG GTTATAGGAA ATGAAATGTG GACATGAATC
  AAAGTTGAAG ATAATTATTT GCCGTTGACT CTTGGTTTTA TTGCATAAGA CAGAAGTAAC
  Y
  AACTAGGATT TAACATTTAA TATTTTAACA AAGAAAACCC ACAGAATAGA CCTTTCATGT
  GATGTAGCAG TCAGGAAGGA ATTTACAGTG AACCACAGAG CCTTCAAACT CAGTGCACAG
  TGTCTGATAC CTAACAACTC ACTGAATACA TTTTGCTTAT TTATTAAAGT AGCTGTCATG
  AGTATTTTAC ACCACTGTTT                                            
  
  Y = C/T
  

  
  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	DBA/2J	FVB/NJ	WSB/EiJ
ss46944206	NES10829663	PERLEGEN	MM_PANEL2	f	SNP	C	C	T
SNP Consensus Information
SNP					Consensus Type	DBA/2J	FVB/NJ	WSB/EiJ
rs30393315					SNP	C	C	T

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
ss46944206	NES10829663	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:53496639 () rs orientation: forward

Symbol	Name	Function Class
Frem2	Fras1 related extracellular matrix protein 2	Intron
Rr576723	regulatory region 576723	942 bp proximal
Rr576724	regulatory region 576724	1030 bp proximal