rs49126906 SNP Detail

Summary

• ID
  rs49126906
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr3:141686852 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        TAAAT AATAAAAGTA TACAGGTTTC
  M
  TGAGTGCTCT AAACAACAAC GCACA                                      
  
  M = A/C
  

  
  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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss136009090	ENSMUSSNP5933069	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	C
ss320997324	CHEV_3_141644055	CHEVERUD	SCREENING_POP	f	SNP				A	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs49126906					SNP	C	C	C	A	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:141686852 () rs orientation: forward

Symbol	Name	Function Class
Bmpr1b	bone morphogenetic protein receptor, type 1B	Intron
Rr586376	regulatory region 586376	598 bp proximal
Rr586377	regulatory region 586377	1030 bp proximal
Rr586378	regulatory region 586378	1163 bp proximal
Tssr35923	transcription start site region 35923	1115 bp downstream
Tssr35924	transcription start site region 35924	1133 bp downstream