rs46690634 SNP Detail

Summary

• ID
  rs46690634
• Variation Type
  SNP
• Alleles
  A

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  138
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:95901268 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        AATAT CAAGGAAAAA CAAGAGAACC
  A
  TGTAAGAGAG GCTCTGTATC TACTA                                      
  
  A = A
  

  
  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
ss144993759	ENSMUSSNP6676212	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A	A
ss324489722	CHEV_13_96534715	CHEVERUD	SCREENING_POP	f	SNP				A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs46690634					SNP	A	A	A	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr13:95901268 () rs orientation: forward

Symbol	Name	Function Class
Gm32702	predicted gene, 32702	328 bp upstream
Iqgap2	IQ motif containing GTPase activating protein 2	within coordinates
Rr484141	regulatory region 484141	401 bp distal
Rr484142	regulatory region 484142	within coordinates
Rr484143	regulatory region 484143	342 bp proximal
Tssr120725	transcription start site region 120725	361 bp upstream
Tssr120726	transcription start site region 120726	565 bp upstream