rs236889830 SNP Detail

Summary

• ID
  rs236889830
• 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
  Chr3:100980588 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    GTTGCAAGA AAGATCCAGG TCCTTTCCTT
  CAGTCACAGA CACTGTCCTG GGCACGGCCA GTTGCAGAGC TGGAAGAGGA AAAACAAGCC
  CATCGAGTGA TCGAGTGACG CGTGTCCCCT CTCCTCCCTT CTCCTTACCT CCCTCATGGT
  Y
  GCCCCTTTAG GTTGATTTAT GGTGTTAAAA TTAGAAGGCT TTGTACAGTT GAAAGTGCTA
  GAGGAATAGT TAATGAATAA ATTCATGACA CACACTAAAT TGGTGTTGGA AAAGAGCAAC
  AAAGAACACC AGTAAAAATC GCCTATGGCT                                 
  
  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
ss320850826	CHEV_3_100877195	CHEVERUD	SCREENING_POP	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs236889830					SNP	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:100980588 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Ptgfrn	prostaglandin F2 receptor negative regulator			Intron
				Noncoding-Transcript-Variant
Rr581952	regulatory region 581952			1650 bp distal