rs234227618 SNP Detail

Summary

• ID
  rs234227618
• 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
  Chr4:104455435 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTGGTGTTCC TGACTCCTGG
  AGCACACTGA CTGGCTGCTG TAGAACAAAG GCATAAGTTC GCCCATTTAG CCATTCAGGA
  GACCTGAGCT CTATGCTGTA CCCCGTGGCT CTAAGCTGTA CCATTTGCCA CACCAGGAAC
  AGCTGAATCA ATCTTTGTTT CCATGGAGCT CAAGCATAGA GAAGAAGGCT AAGAAAACAA
  R
  GTTAGCAAAA CACCACGAGT GCCAAAACAG ATGCCAAAAA TGGATAAAGT GAAAAAGTAT
  GCAAGCCTAT TAAGAACATG CAGGGCACCA GGAATTCAGT GGTCAGCTGA CCCAACAGAG
  ACTTTTCCTT GATTGGAGTT CATGGCCTAA TAAGGAGGAG AGCTGTTAAG CAGATTAGTG
  CAAATGAGAT TAATCTACTG                                            
  
  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
ss321241253	CHEV_4_104270843	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs234227618					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:104455435 () 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			343 bp distal
Rr596484	regulatory region 596484			within coordinates