rs29119655 SNP Detail

Summary

• ID
  rs29119655
• 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:127478267 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCCATGAAGA AATATTTAGT
  TTTATTTTCC CTGTTATTAG TCAAAATAAA AATGGAATAA TTACTGAAAC GAATTTCTAA
  GAAAAAAAAC AGCAGATCTG GATTATTTGT ATAATTTAAT TCTTTAGTTC TTCAGTTTTC
  ACTCTGGCAG TGGAAATGTG ACCTTTTAAT GCAATGGCTT AGCACAGCTG AAATGGCTCA
  Y
  GTTGTCAGGA ATGAAAGAGG GGCCAGTCAA ATTCAAATGA TCGAGTTCTC TAATTACTGG
  ACCCTATAGT GGAGCACCTG CTTGCACTCC ATCCCTGCCC CTACACACTC CAGTGCCTAG
  CCTTTTTTTG GAAAACTTAA TGTACTTGGT AGTCAGCCCA TTGCTCTAGA GAACAAAAAA
  GAAAGATGCT CGCTGAAATC                                            
  
  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	KK/HlJ	MOLF/EiJ	PWD/PhJ
ss38444888	NES09792033	PERLEGEN	MM_PANEL2	f	SNP	C	T	T
SNP Consensus Information
SNP					Consensus Type	KK/HlJ	MOLF/EiJ	PWD/PhJ
rs29119655					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
ss38444888	NES09792033	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:127478267 () rs orientation: forward

Symbol	Name	Function Class
Rr2779	regulatory region 2779	867 bp distal
Rr9113	regulatory region 9113	within coordinates
Rr395642	regulatory region 395642	346 bp downstream