rs29918751 SNP Detail

Summary

• ID
  rs29918751
• Variation Type
  SNP
• Alleles
  A/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:145401735 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AATGAAGCTG ATTATGAAAT AAAAAAAAAC TTAAGATAAA
  GACTCTTTCA AGCAGTGGGC AAGGAGTGGC TCATCATATT CAGGGGCACT TCCATGAACC
  W
  ACTGGTGAGT TAGTTCTCAC AGAACCTTGT AGATTAGAAA GGAGAGGGAT GGGATATTCA
  AAGGGCTAAA AGATACTGCC AATCAGGAAT GGTCTGCAA                       
  
  W = A/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	129X1/SvJ	A/J	C57BL/6J
ss45376780	mCV23985236	ABI	CRAMUS_MOUSE	f	SNP	A	T	T
ss147835229	ENSMUSSNP6022586	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	C57BL/6J
rs29918751					SNP	A	T	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:145401735 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr566544	regulatory region 566544			1970 bp distal
Slc24a3	solute carrier family 24 (sodium/potassium/calcium exchanger), member 3			Intron
				Noncoding-Transcript-Variant