rs48718266 SNP Detail

Summary

• ID
  rs48718266
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr6:83727596 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        AGTCA TCGCTGAAAA TCTAAGAAGG
  R
  AAACCTTGGG AGAGTGGCTC CACCC                                      
  
  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	DBA/2J	LG/J	SM/J
ss133350010	ENSMUSSNP6915535	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
ss321844744	CHEV_6_83700608	CHEVERUD	SCREENING_POP	f	SNP		G	A
SNP Consensus Information
SNP					Consensus Type	DBA/2J	LG/J	SM/J
rs48718266					SNP	A	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:83727596 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Atp6v1b1	ATPase, H+ transporting, lysosomal V1 subunit B1			Intron
				mRNA-UTR
				Noncoding-Transcript-Variant
Gm66892	predicted gene, 66892			within coordinates
Rr632931	regulatory region 632931			within coordinates
Rr632932	regulatory region 632932			112 bp distal