rs50899356 SNP Detail

Summary

• ID
  rs50899356
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr3:116836577 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TAAATAATAT TTTTCCAATA
  AATGAATAAA TTAATGTGAA TTAGTATTGA AAGAAGATTT ACATGGACTC ATGATGGCTT
  TTATTAAGGA TTATGTTAAA AACTTGCTTT GGTAGTCTGT GGCCCAGGGC TTGTACCACA
  CAGTAAAGTT AGAGAGACAC AGATTGGGTG TAGTCGCAAG TAGTGATCCT GTAGTGTTTC
  R
  GTTTGCTCTA AGGTAACCCA GGGAACCTGA AATATCTAGT TATGGATTGT GCTATTTGAT
  ATTGATTGTT GATGTGACAA GACCTGGACT CATTTGGGAT ACAAACCTCT GGGGGTTTCT
  ATGAAGCGTT ACCTAGGTTA GGTTAGCTGA GATGGGAAGA TTCATTCTGT GAGTGCATCC
  ATGCCATGAA CTGGGGTCTC                                            
  
  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	BTBR T<+> Itpr3/J	CAST/EiJ	KK/HlJ	NOD/ShiLtJ	PWD/PhJ	WSB/EiJ
ss60435224	NES15935707	PERLEGEN	MM_PANEL2	f	SNP	A	G	A	A	A	A
SNP Consensus Information
SNP					Consensus Type	BTBR T<+> Itpr3/J	CAST/EiJ	KK/HlJ	NOD/ShiLtJ	PWD/PhJ	WSB/EiJ
rs50899356					SNP	A	G	A	A	A	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
ss60435224	NES15935707	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:116836577 () rs orientation: forward

Symbol	Name	Function Class
Rr583826	regulatory region 583826	1370 bp proximal