rs48447360 SNP Detail

Summary

• ID
  rs48447360
• 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:111860957 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCTTGTAAAC CAAGACATTG
  GCTCATTACT ATATATAATG ATAGCTACAC TTCACAAATA GAGCACAATC ATTTATCGAT
  CCAACCCACT CTCTCCTTGC TGGCAAATCA AAACATGATC AGAAGTTTGT TTGGCAAGTT
  CAGACAAAAT AGAATGATCT GTGTGATTTG GCTGACTAGT AATCTCAAAA GCTGTGTCTA
  Y
  ACTTTGCCAG ATCACAAAAT GCAAATGAGC TATCCATGAT TCATTATTCA GTACCACACT
  CCATGAAATG AGGATAACAA TAAGTGCCTA CTACTGCACT AGATTTTTGT TGAGATAAGT
  TTTTTTTTCT TAACTACTGC AAAGTACTCA CAATGTCTGG CATGTAACGA ATGCTTTAAT
  ATATAATCTA TCACTTTTAT                                            
  
  Y = C/T
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

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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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss134277776	ENSMUSSNP6556215	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	T	C
ss325913361	CHEV_X_110064869	CHEVERUD	SCREENING_POP	f	SNP				T	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs48447360					SNP	T	T	C	T	C