rs261577462 SNP Detail

Summary

• ID
  rs261577462
• 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
  Chr10:111274210 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    ATAGCTATA AATAGAGCAA TTCTTTTCAA
  ACCACCTCCA AAGGTACACT TTCTTCAGAT TAAAAAGTAT TTACTTAAAT TAGGCAAGAA
  ACCAGAACTA AGCCTAGAAA ATTATTTCAG TACTGACTAA TGTCACCACT TTATTTTTAA
  M
  CTATATGATG GATCATAATA GAAACTTATT TTTAAATTCT AAAATGACTA ATTTTCTTTG
  CGTAAGGGAA ACTATTTTAA AATTAAGTCT AATATTATGA TAACTTACTT TAATGTAAAA
  TTGAGGGAAG AATTTTATTG AGTATTGTGG                                 
  
  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
ss323473586	CHEV_10_110875405	CHEVERUD	SCREENING_POP	f	SNP	A	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs261577462					SNP	A	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:111274210 () rs orientation: forward

Symbol	Name	Function Class
Rr229875	regulatory region 229875	1081 bp proximal