rs29295905 SNP Detail

Summary

• ID
  rs29295905
• 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:150916208 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TGAAGAATAA GAGGCAGTAA
  GTATGCAAAA GTGAGAAAGC AGCTTTCCAT GACAGCAAAT GGACAGCCCA CGGGCAGAAC
  ATTTGTTCCT TGAGGGCACA GTTTATCTCC TGTCTACTAT TGTATGGCTC CAGGCTTCTG
  AAACAGAGAT GTGAAAATCT GTTCGACTAG AAGTGAATGG TATTTTGTCA TAGAAAGTAT
  Y
  ACAGTGTTAG AAGGCCTAAC GTATAGTTTC AGCACTTTGG AACAATTCTG CTGAGTTCAA
  TTTCCCAACT GTTAATTGTA TACCCACCAT GTGCAAGGTG CCAACATGAA GCCTTGTGGA
  AGAATTGAAA GAAAACTTGG TTTTGCCCTT GAGCAACTCT TAGTGAGGTG AAACAGGCAA
  TGGGTTGACT AGTCCCTTCC                                            
  
  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
ss38488868	NES09735414	PERLEGEN	MM_PANEL2	f	SNP	T	C	C
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ	PWD/PhJ
rs29295905					SNP	T	C	C

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
ss38488868	NES09735414	PERLEGEN	MM_PANEL	f	SNP	C/T