rs261096930 SNP Detail

Summary

• ID
  rs261096930
• 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
  Chr10:61357372 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGGTATTTTC CTCGTTTACA
  TTTTCAATGC TATCCCAAAA GTCCCCCATA CCCACCCCCC CAATCCCCTA CCCACCCTTA
  CAGACTTTTT TGCATAATCC ATTGTTTGCC TTATTTTTCT TAGAAAGATT CAAGTGTGTG
  TGTGTGTCTT TGCATGTGCT ATGTGTGTGC AGTGTTCTTG GAGGCCACCG AGGGTATTGG
  M
  TCTCTTGGAG TTGGAGGTCC AGGTGGATGG GAGCTGCTCT GCCATGGAAG TGCAGGGAGT
  TAACCGTGAG GCCTCTGGAA GAGCAGCAAG CCCCATTAGC TGCTTTGCCG CTTCCTAGCC
  CCTCGTCTAT CTTTTACAAC ATTCCTGCCT TATAGACTCT CTAAGTTTGG AAAGATACCT
  TCGCCTAAGA GCTTACATAG                                            
  
  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
ss323328680	CHEV_10_60984341	CHEVERUD	SCREENING_POP	f	SNP	A	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs261096930					SNP	A	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:61357372 () rs orientation: forward

Symbol	Name	Function Class
Lrrc20	leucine rich repeat containing 20	within coordinates
Rr215563	regulatory region 215563	1029 bp proximal