rs107707632 SNP Detail

Summary

• ID
  rs107707632
• Variation Type
  SNP
• Alleles
  C/G

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:85304742 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      A GGTATGCTGA TGTTCTCTCT CTTTCTCTCT CTGTGTCTGT
  CTGTCTGTCT GTCTGTCTGT CTCTGTCTCT GTCTCTCACT CTGCCTCTCT CTCTGTCTCT
  S
  TCTCTGTCTC TGTCTCTCTC TCTCTCTCTC TCTCTCTCTC TCTCTCTCTC TCTGTCTCTC
  TCTCTCTCTC TGTCTGACTC TTCGCCTCAT CACCCCCAAA T                    
  
  S = C/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
ss144854167	ENSMUSSNP2051220	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs107707632					SNP	C	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:85304742 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm2619	predicted gene 2619			Intron
				Noncoding-Transcript-Variant
Gm16025	predicted gene 16025			within coordinates
Rr414357	regulatory region 414357			317 bp proximal
Tssr137	transcription start site region 137			305 bp downstream