rs29295908 SNP Detail

Summary

• ID
  rs29295908
• Variation Type
  SNP
• Alleles
  A/G

• 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:150915869 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CACACTAAAT TGTAATTATG
  ATATATGTAT CTATATATTC GGGTGTTAGT CCAGGCATCC AAAAAGTATG GATTGCTTAT
  TGCTTACCTA CCATGTACCA GGATTTTTAC TATACCTATG ACATTGAACG TGAAGTGTAA
  CAATAGACAG AGAAACACCT ACCCTTGAGT GTTAACAGTT CGAAGAAGGA AACAGATGGT
  R
  AGCAACAAAG AACTGCACCA GTCAATATGC AATTATAAAC TTGCTGTGCT GAGCAAAGAA
  AAGGACTCTC AGACAGCATC TATCGAGGGA CCTACCTACA CTAAGAAGGA GAGAAAGGGC
  TGCTGATGAA CTAAGATCTG AAGAATAAGA GGCAGTAAGT ATGCAAAAGT GAGAAAGCAG
  CTTTCCATGA CAGCAAATGG                                            
  
  R = A/G
  

  
  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	WSB/EiJ
ss38488871	NES09735411	PERLEGEN	MM_PANEL2	f	SNP	A	G	G	G
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ	PWD/PhJ	WSB/EiJ
rs29295908					SNP	A	G	G	G

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
ss38488871	NES09735411	PERLEGEN	MM_PANEL	f	SNP	A/G