rs233635699 SNP Detail

Summary

• ID
  rs233635699
• Variation Type
  SNP
• Alleles
  A/C

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

Genome Location and Flanking Sequence

• Location
  ChrX:120754028 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCGGTGAAAT AGCTGAATAT
  AAAATTAACT CAAACAAGTC AATGGCTTTT CTCTACACAA AGAATAAACA GGCTGAGAAA
  GAAATTAGGG AAGCAAAAAC CTTTCTCAAT AGTCACAAAT ATTATAAAAT ATCTTGGTGT
  GACTCTAACT AATGAAGTAA AAGGTCTGTA TGATAAGAAC TTCATGTCTC TGAAGATATA
  M
  ATTAAAGAAG ATCTTAGAAG ATGGAAAGAT CTGCCATGCT CATGGATTGG CAGGATCAAT
  ATTATAAAAA TGGCTATCTT GCTAAAAGCA ATCTACATAT TCAATGCAAT ACCCATCAAA
  TTTCCAACTC AGTTCTTCAA TGAATTAGAA AGAGCAATCT GCAAATTTAT CTGGAATAAC
  AAAAAAACCT AGGATAGCAA                                            
  
  M = A/C
  

  
  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
ss325960944	CHEV_X_118957940	CHEVERUD	SCREENING_POP	f	SNP	A	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs233635699					SNP	A	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:120754028 () rs orientation: forward

Symbol	Name	Function Class
Rr395603	regulatory region 395603	1682 bp upstream