rs30926370 SNP Detail

Summary

• ID
  rs30926370
• Variation Type
  SNP
• Alleles
  A/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
  Chr3:138355706 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAGAGAAAAA AATAACATGC
  TAGGAAAAAT ATTTGCAGTG TGTGGAAAAA AATGCTTATT TAAATATAAA GGTGGTTTCC
  CCAAGCTTGT GAGGGGGGAG GGGCTCCCCG GCAGAAAATC AACAAGAAGC ATCAGTGCTC
  AGGAAAGAAA GGGGGGAAGA GGGGGGAGAC TGAAATATCA AAGCACAATC ACGTGTATGT
  W
  CTAACTGACG GAAAGTTCAG CATGCTCTTA CCGTGTTCCA TGTGTTGTCT TGGTCTGTGT
  GTCCACGGTG AAATTATCAA GTCAAAGGCA TTGATTATTA AATTATTAAA TCTAGCATTG
  CCCCCCCCCC CGCACCTATG TATATTTTCA TGTGGTGAAA ATGTTTAAGA TCTCTCTTAG
  CAACTGTCAA TCATGTGATA                                            
  
  W = A/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	C3H/HeJ	CAST/EiJ
ss46998874	NES10882621	PERLEGEN	MM_PANEL2	f	SNP	T	T	A
SNP Consensus Information
SNP					Consensus Type	A/J	C3H/HeJ	CAST/EiJ
rs30926370					SNP	T	T	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
ss46998874	NES10882621	PERLEGEN	MM_PANEL	f	SNP	A/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:138355706 () rs orientation: forward

Symbol	Name	Function Class
Rr586176	regulatory region 586176	1497 bp proximal
Rr586177	regulatory region 586177	1853 bp proximal