rs30906356 SNP Detail

Summary

• ID
  rs30906356
• 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
  

Genome Location and Flanking Sequence

• Location
  Chr3:137954776 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAACTTTACA ACAGAAAGAG
  CTGTTCTCAG CCAGTTGTAA AAGGGCCAGA GAACAATGTG TGCTCTGCAG CTCTCCAAAT
  GATTCTAATC TCCGGTTAGG AGCCCCCTGT AGAAGTCATC TGTGGAGACA TCCATCCTTT
  CCATCTGGTG GACTTCCCTC CACCGTGCTC TGCCAAAGTA TTGTGTAACT TCTGCTAGCG
  Y
  GTCTCCAAGT CCGATAAATC ATACCTCGTC CCATAATTAT AGTCAACAGC TGGGAAAATA
  AATAGCAAAG GACGCCAGTG GACATGGATA CAGGATGATG TAGAAATGGT ACTCACACAA
  TGAAGAATGG TCAATGTCAA TTCAACAGGG AAACAAGAAG GTCTAGACGC CAAGCATCAC
  ATGAGACTAC ACAGCCTCTT                                            
  
  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	A/J	BALB/cByJ	C3H/HeJ	CAST/EiJ	MOLF/EiJ	WSB/EiJ
ss46996298	NES10868763	PERLEGEN	MM_PANEL2	f	SNP	C	C	C	T	C	T
SNP Consensus Information
SNP					Consensus Type	A/J	BALB/cByJ	C3H/HeJ	CAST/EiJ	MOLF/EiJ	WSB/EiJ
rs30906356					SNP	C	C	C	T	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
ss46996298	NES10868763	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:137954776 () rs orientation: forward

Symbol	Name	Function Class
Rr586105	regulatory region 586105	within coordinates