rs29295561 SNP Detail

Summary

• ID
  rs29295561
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  ChrX:150917372 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTGGATATTT GAAGATAGTA
  ATCATTTCCT TAGACGCCTG CTTTCCTTTA GGCCAAATAT CTGTTTCTTG AAAGGTTCGT
  CATTGTTTTA AATCCCCTTA GCATCTGTAA ATATAGTTTA GTTTATGTGA GATTTATATT
  TCACCCACTT TAAAGAGGAT ATTAGGCGAC TCATCAGTTT ATAACATGAA AGAAAGAAAA
  Y
  TGGGGATAAA AATATGGAAG AAAACAGACC AGCAACTATG GAAAAGAAGC ACAAATAGAT
  GTTGCCAGGT ACCTAAAATG AACTGAATTA TAATTGGACT CTGAATTTGG CTCAAAGTTT
  TATGGCAGCC AGGACAAAAT TGGAAACATG ATGGGTTATG TGGTTTTATG TTCTGACAGG
  ATCAAGCTTA CACATCATCT                                            
  
  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	CAST/EiJ	MOLF/EiJ	PWD/PhJ
ss38488864	NES09735348	PERLEGEN	MM_PANEL2	f	SNP	C	T	T
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ	PWD/PhJ
rs29295561					SNP	C	T	T

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss38488864	NES09735348	PERLEGEN	MM_PANEL	f	SNP	C/T