rs47077674 SNP Detail

Summary

• ID
  rs47077674
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  ChrX:120755354 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    taggtccca acaagtaaga agaacacatg
  ttcaactatg ttcatagcat ccttatttat aatagccaga agctgaaaag aacccacatg
  cccctcaaca gaggaatgga tacaaaaaaa tgtggtacct ttacacattg gagtactact
  Y
  agctattaaa atgaatgaat ttatgaaatt cctaggcaaa tggttggacc tggagggcct
  catcctgagt gaggtaattt aatcacaaaa gaactcaaat gatatgtact ctctgatcag
  tggatattat cccataaact tagaatgccc                                 
  
  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	A/J	LG/J	SM/J
ss134396156	ENSMUSSNP2982261	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
ss325960954	CHEV_X_118959266	CHEVERUD	SCREENING_POP	f	SNP		T	C
SNP Consensus Information
SNP					Consensus Type	A/J	LG/J	SM/J
rs47077674					SNP	T	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:120755354 () rs orientation: forward

Symbol	Name	Function Class
Rr395603	regulatory region 395603	356 bp upstream