rs31336600 SNP Detail

Summary

• ID
  rs31336600
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr14:70007752 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAGGAAGTCT TCCTGCCTCA
  GGATCCGAGT CACAGGTGTG CCCTCCATTT CTGGATTGTA GTTCATTCCA AATGTAGTCT
  AGTTGACAAC TGAGAATAGT CATCACAACA CTAAGTGACT TCAGGTGAGT GCAATACCAT
  AGAATGTGTC TGGAGATCAG AGGCCGGCTT CAGGTGTCAG TTCCCACTGT CTACCTCATT
  Y
  GGAACAGGCA GGATCTCTCT TGTTCGGCAC TGAGTATGCT GCTGGCTGTC CCATGAGCTT
  CTAGGAATTC TTCATCTCCT CCTCCCATTC AGCCAGAGGA GTCCTGGGAT TTCAGATGTG
  TACTGTTGTG TCTGGCTTTA TATTGAGTTT TGGGAATCTG AACTCAGGTC CTTGCGATTG
  TGTGGCAAGT GTATTTATCC                                            
  
  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	129X1/SvJ	A/J	DBA/2J
ss39278502	mCV22654476	ABI	CRAMUS_MOUSE	f	SNP	C	T	T
ss139676569	ENSMUSSNP1116410	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs31336600					SNP	C	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr14:70007752 () rs orientation: forward

Symbol	Name	Function Class
Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	Intron