rs46513239 SNP Detail

Summary

• ID
  rs46513239
• Variation Type
  SNP
• Alleles
  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
  Chr1:135716982 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        ACCTG AGTTCAATCT CTAGGACCCA
  C
  GTGGTGGAGG GAGACAATCA ACTCT                                      
  
  C = 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	A/J	LG/J	SM/J
ss145546347	ENSMUSSNP1895094	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
ss319993387	CHEV_1_137685821	CHEVERUD	SCREENING_POP	f	SNP		C	C
SNP Consensus Information
SNP					Consensus Type	A/J	LG/J	SM/J
rs46513239					SNP	C	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:135716982 () rs orientation: forward

Symbol	Name	Function Class
Rr419276	regulatory region 419276	951 bp distal
Rr419277	regulatory region 419277	1244 bp distal
Rr419278	regulatory region 419278	94 bp distal
Rr419279	regulatory region 419279	276 bp distal
Rr419280	regulatory region 419280	490 bp proximal
Rr419281	regulatory region 419281	761 bp proximal
Tnni1	troponin I, skeletal, slow 1	Intron