rs265344174 SNP Detail

Summary

• ID
  rs265344174
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr3:115817642 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    ttaaagaat tgacaaacat atatttttaa
  gagaaTGTAA GACCACATTT TTTTAATATT TGTCAGGCCA AATCACTTTA CAAATGAATG
  TAAATCCCTG ACAAGAGTGG TCAGTGACTT AACTGAAACA TAATGACTGT ATTTTATTGC
  Y
  GTCTCTACTC CAGGGGTTGC CACATCTGCA AACTTCCGGG AAGAGTCATG GGGATTCGAG
  TGCTCCGGTT CTCCCTGGTG GTCATCCTTG TGTTGCTGCT GGTAGCGGGG GCTTTGACCA
  ACTTACTCCC CAACATCAAA GAAGACAAGA                                 
  
  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	LG/J	SM/J
ss320893973	CHEV_3_115726911	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs265344174					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:115817642 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Extl2	exostosin-like glycosyltransferase 2			Intron
				Noncoding-Transcript-Variant
Rr583641	regulatory region 583641			1817 bp proximal