rs255296600 SNP Detail

Summary

• ID
  rs255296600
• 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
  Chr4:104454888 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    CAACCAACC TGGGGTGGGA GGCCATGCCT
  GTCTCCAGTA GACTCTGTGG CCAATTCCCT TGTGTTATAG AAGTGCTAAT CACCTCCCTT
  CCTGGAACCT GACTCCTGGA GGTGTTTGTT TATAATGAAG TGTCTGCAGT GCAACTTTGA
  R
  TGTCAGACTT CAATATTGAC AGTGCCTCCT GCTCCAGAAC AAGGAACCTC CAATGGCCTC
  TGTGAGGCCT GTTCAAACTG GGCTGTTGGC TCCATGCCTA AGAAATGAGC CTGATTTAAA
  TTCAGGAAAG AGTGCACCTC CAGTCTAGAG                                 
  
  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
ss321241248	CHEV_4_104270296	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs255296600					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:104454888 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dab1	disabled 1			Intron
				Noncoding-Transcript-Variant
Rr596483	regulatory region 596483			within coordinates
Rr596484	regulatory region 596484			372 bp proximal