rs50795907 SNP Detail

Summary

• ID
  rs50795907
• Variation Type
  SNP
• Alleles
  A/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
  Chr16:94353106 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACAAAGTCAG CTGGATGGCC
  TTGAGCCACC CCACTGTAAA GGTGAAATGG TTCTGCCCTG CTGACTTGGC TTGGAGCCCC
  CACCATGATG GTGACATGGT TCAGCCTGCC AAGTGGGGGA GGGGAGGAGC TAGAGATGTC
  TTTATAGCTA TTGGACCTTT GAGAGCTCTC TCTTTTGGCT TGGAAGGAGC TCTGGGTATG
  W
  GTTAGGCATT TTCTCTCTGG GCTTGCAGGA ACAACAGAGA AGCAGCTGGT AGGACACAGA
  ATAGGATTCT AGGAGAGAGC TGAGGAGCCC TCTTGGGTTT GGAGGAGCTC AAGAGAAAGG
  TAGACTAGCT CAGTAGAATA ACACAAATAG AAAGAGATTT CTAAAGAGCT ATCAGGTTAG
  TTGTAGGATC ACCCTTGTAA                                            
  
  W = A/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	A/J	PWD/PhJ
ss60514792	NES16523668	PERLEGEN	MM_PANEL2	f	SNP	T	A
SNP Consensus Information
SNP					Consensus Type	A/J	PWD/PhJ
rs50795907					SNP	T	A

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
ss60514792	NES16523668	PERLEGEN	MM_PANEL	f	SNP	A/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr16:94353106 () rs orientation: forward

Symbol	Name	Function Class
Gm56630	predicted gene, 56630	within coordinates
Rr328341	regulatory region 328341	within coordinates
Rr392165	regulatory region 392165	within coordinates
Tssr139557	transcription start site region 139557	23 bp downstream