rs237217102 SNP Detail

Summary

• ID
  rs237217102
• Variation Type
  SNP
• Alleles
  C/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
  Chr4:104455294 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    TTTATTTGT TGGAGACTAG GTGAATCACG
  AGGTTGGGTA AAGTAGGGTG TGTGTGGGAG GCGTTTTTCC TGACTTCTTT GAGGCTTTCC
  CTTGGTGTTC CTGACTCCTG GAGCACACTG ACTGGCTGCT GTAGAACAAA GGCATAAGTT
  Y
  GCCCATTTAG CCATTCAGGA GACCTGAGCT CTATGCTGTA CCCCGTGGCT CTAAGCTGTA
  CCATTTGCCA CACCAGGAAC AGCTGAATCA ATCTTTGTTT CCATGGAGCT CAAGCATAGA
  GAAGAAGGCT AAGAAAACAA GGTTAGCAAA                                 
  
  Y = C/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
ss321241250	CHEV_4_104270702	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs237217102					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:104455294 () 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			202 bp distal
Rr596484	regulatory region 596484			within coordinates