rs51681319 SNP Detail

Summary

• ID
  rs51681319
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr10:89620270 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CCATCCTTTT GTCTCAGCTC CAAACTTTGT CTCTGTAACT
  CCTTCCATGG GTGATTTTTT CCAATTCTAA GAAGGGGCAA AGTGTCCACA CTTTGGTCTT
  Y
  GTTCTTCTTC AGTTTCATGT GTTTTACAAA TTGTATCTTA TATCTCGGGT ATACTAAGTT
  TCTGGGCTAA TATCCACTTA TCAGTGAATA CATATTGTG                       
  
  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	DBA/2J
ss147261968	ENSMUSSNP5768343	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J
rs51681319					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:89620270 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Bltp3b	bridge-like lipid transfer protein family member 3B			Intron
				Noncoding-Transcript-Variant
Tssr95182	transcription start site region 95182			1429 bp upstream