rs46014960 SNP Detail

Summary

• ID
  rs46014960
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr10:24845684 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGGAACACAC ACACATCCCA
  AAAGTTATTT GGCCAAAGTG TCATTGAGTC ATGGTTGAAA AATTCTGGTG TAGTCTGCAT
  AGCTATGTTG GAGTGAGCAC CACCTTTAAA AGATTAGACT GTTTTGCAGA GCCTGCTCCC
  TGTCCCTGAT CCCAACATCA TAGACCTGAG TACTTGGCCT TTTCTCTAGC CAAGCACTGG
  Y
  TTTCCCAGTG GTCACTTTCT TATGCTCAGG ACTCTGGCAG CCCATCATTC GCTTGGAAAT
  CCTAAAGAGT TCTGCAGTTT TTTTCTTTTT TAAAAATCTT TAACTCATTT TTCTTCTTTT
  CTTATCTGCA AAAACCTGAA TGAGACTTGT TTCTTTCCAT TAAGTGTTAG GGGTTAGATT
  TAGGGTTGTT TTAATATTTA                                            
  
  Y = C/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	PWD/PhJ	WSB/EiJ
ss61262274	NES16878953	PERLEGEN	MM_PANEL2	f	SNP	C	T	C
SNP Consensus Information
SNP					Consensus Type	A/J	PWD/PhJ	WSB/EiJ
rs46014960					SNP	C	T	C

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
ss61262274	NES16878953	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:24845684 () rs orientation: forward

Symbol	Name	Function Class
Gm68022	predicted gene, 68022	668 bp downstream