rs47298268 SNP Detail

Summary

• ID
  rs47298268
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr6:118602067 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GTGCTGCCTT ATAGAACCTG GAAAGACTCA GCGGGAGTCT
  TGAAGGCTGG AGGAACTCTG GCTGAGGGAA CAGAGAGGGC AGAGGGCCCC TGGGAAGGGG
  R
  CTCCTGAAGA GGACTGCATG GTTGATGGAC AGTGCCTTCT CTTCTCTCCC CACCTCAAAT
  CATGCATATC CATCAAAGCA GGGGATGCTG GTGGGACAC                       
  
  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
ss133584438	ENSMUSSNP6805445	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs47298268					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:118602067 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit			Intron
				Noncoding-Transcript-Variant
Rr637498	regulatory region 637498			1233 bp proximal
Rr637499	regulatory region 637499			1337 bp proximal