rs13468076 SNP Detail

Summary

• ID
  rs13468076
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  121
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:135679786 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

             GGGCTCCCCG TGATCGAGGC CACCAGCTTT GTTTCTCCCA AGTGGGTGCC
  R
  CAGGTGAGCC CAGGCTCTGG GAGGAGCCTC TTCCAGGTGG GAGGAGCCTG           
  
  R = A/G
  

  
  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
ss147554643	ENSMUSSNP4034744	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs13468076					SNP	G	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:135679786 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Hmgcl	3-hydroxy-3-methylglutaryl-Coenzyme A lyase			Coding-Synonymous
				Intron
				mRNA-UTR
				Noncoding-Transcript-Variant
				Splice-Site
Rr398602	regulatory region 398602			1828 bp upstream
Rr602216	regulatory region 602216			773 bp distal
Rr602217	regulatory region 602217			720 bp proximal
Rr602218	regulatory region 602218			1863 bp proximal
Rr602219	regulatory region 602219			1964 bp proximal