rs45772386 SNP Detail

Summary

• ID
  rs45772386
• Variation Type
  SNP
• Alleles
  A

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

Genome Location and Flanking Sequence

• Location
  Chr14:70010908 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCAGGCAGTC CCTCAGTTGT
  GATAGCCATT TCCCAAGTAT GTCTAACTAG GGCACGCGTC TTCACCACAG CTCTGGGAAT
  CCCGAAGTTT GCTTAATCAG TTTTCTTTCC ATCCTCAGGC CAGTACCTGT CAGAAGGGAA
  CTGCAAGCCT TGCAGAGAGG GTATTGACTA CACCAGCCAT TCCAACCATT CTCTGGATTC
  A
  TGTATTCTCT GCACAGTCTG TAAGGAAGGT ACAGAGCAAA GGGGCCCTTC CCACAGGAGG
  AGCATGGGCA GGGGGATTCA TAACTGCAGT GAACTGGAAA ACTTCAGTTC CAGCCATCTT
  GATCTTCATT TTTCCCTGTT CTCCGCCTGT CTTTAGTTCA ATGGGACAAA ACCACAAGTT
  GTGCTGTGTT TTAGGAATCA                                            
  
  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	A/J
ss139676602	ENSMUSSNP2605822	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	A/J
rs45772386					SNP	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr14:70010908 () rs orientation: forward

Symbol	Name	Function Class
Rr494754	regulatory region 494754	570 bp proximal
Tnfrsf10b	tumor necrosis factor receptor superfamily, member 10b	Coding-Synonymous
Tssr126377	transcription start site region 126377	1649 bp upstream
Tssr126378	transcription start site region 126378	1698 bp upstream