rs263008984 SNP Detail

Summary

• ID
  rs263008984
• Variation Type
  SNP
• Alleles
  A/G

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

Genome Location and Flanking Sequence

• Location
  Chr4:87130175 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    AGATGTTTC CTGGGCCCCT AGGAAGCCCC
  TAGAGCTTTG AACTAATTAT GCATTAAAAG TATAATCACG TGGTTAAGCT GTTCTCCATC
  CTCAGACTGT GCTCATTGAT CAGGTTGGTG GAGTTACAAC ATTAGCTCAT GCTAGACAAT
  R
  CCACAGTAGC TCTCTTCTTA GACTATATAG GTGTATATAG CAATTAGCTT CAATGCCTTG
  TTCAAGAAAG ATGCAAATGT TACTAGGGCA TGGAATGGGA AGGGCTacac acacacacac
  acacacacac acacacacac acacacacac                                 
  
  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	LG/J	SM/J
ss321200596	CHEV_4_86857842	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs263008984					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:87130175 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr594869	regulatory region 594869			980 bp distal
Rr594870	regulatory region 594870			164 bp distal
Slc24a2	solute carrier family 24 (sodium/potassium/calcium exchanger), member 2			Intron
				Noncoding-Transcript-Variant