rs215124668 SNP Detail

Summary

• ID
  rs215124668
• Variation Type
  SNP
• Alleles
  G/T

• 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
  Chr4:103900831 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    ATCAACTAT TTAAAAAAAA AAAATACTTG
  CTGAACGGTG AAGTTACATA AGAGCTCTTA AAAGAAACTC AAGTCCTAGA AGGGGCTGTC
  ACAATATTGA GATGATGCCC AGACCAGCTT ACAGCAAGGG AACTGGCTGT TCTCAACCAT
  K
  CATGTTGAAT GATTTGCTTC AGCGATCCAG AATATTCCCT ACCCCCACTC CCCCATCCCT
  CCATCCCCAC ACTGTTTATA AGCCTGACTG CAGACAGTGA TGTTCAGGCC TGGAACTAAA
  ATCAATCTAT TTATTGTAAT GACTTCTAGT                                 
  
  K = G/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	LG/J	SM/J
ss321239454	CHEV_4_103716239	CHEVERUD	SCREENING_POP	f	SNP	T	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs215124668					SNP	T	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:103900831 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dab1	disabled 1			Intron
				Noncoding-Transcript-Variant
Rr596428	regulatory region 596428			within coordinates
Rr596429	regulatory region 596429			1055 bp proximal