rs261019660 SNP Detail

Summary

• ID
  rs261019660
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr3:141686188 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCTGTATCCT AGTACAGAGA
  CATCTGCTAA TTCACGTTCA GGAATGCTTT CTCACAACAG GTAGAATATG GAAACAGCCT
  ATATATATAT ATCCTGCAAC TGATAATTTT GAAACCTTTT TTAAAATTAT GCAGCCAGAC
  AGTGGTGGAG AACGTCTTTA ATCCCAGCAC TCTGGGAGGC AGAGGCAGGC AGATCTCTGA
  R
  CTTAAGGTCA GCCTAGTGTA CAGAGCCAGT TCCAGGACAG CCAGGGTGAC ACAGAGAAAC
  CCTCTCTAGA CACCCCTACC AAAATAATGC ATGCACTTTG GGTATGGTCA TGACACTTCA
  TACCAGGAAG CTGAGGTGGA GACTAGTATA GCATGAACAC CCAGTACCAG ATCGGTCATG
  GCTACACAAA AAGATCAAAT                                            
  
  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	LG/J	SM/J
ss320997313	CHEV_3_141643391	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs261019660					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:141686188 () rs orientation: forward

Symbol	Name	Function Class
Bmpr1b	bone morphogenetic protein receptor, type 1B	Intron
Rr586376	regulatory region 586376	1262 bp proximal
Rr586377	regulatory region 586377	1694 bp proximal
Rr586378	regulatory region 586378	1827 bp proximal
Tssr35923	transcription start site region 35923	1779 bp downstream
Tssr35924	transcription start site region 35924	1797 bp downstream