rs50672238 SNP Detail

Summary

• ID
  rs50672238
• Variation Type
  SNP
• Alleles
  C/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
  Chr16:85850599 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATTATATCAG TATGGTTCCT
  GTTAGAATAA AACACAAGAA GCCAGGTGTT TTGCAACAAT AACGACAATG AAATTAACAA
  TAACAACAAC AACAACAAAA GGCCAATTTA GTTTTGTACG TGGTCTATTG CCACTGAAGG
  GATTGTGGCA AATGGAAAGA ACTCTAAGAA GCAATGCATA AGAGAATACA CAGCAAACTG
  Y
  AATGTCCAGG CATGTTAGAT GCTAGGTTTG TCCTTATTTG CAGCTATCCA TCCTTGAGGT
  AATAGGTTAT CTGTATAAGT TTTATGCATT TAGGGCACAG TCAACTTCTT TATTCTTAAA
  TTTTATTCCT TGAAAATGGT ATACATGTCT ACACTTCATC TTGTTTATAT CTACCATCTC
  AGCCCACAAC TGCTTAGAAT                                            
  
  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	PWD/PhJ
ss60244869	NES15748710	PERLEGEN	MM_PANEL2	f	SNP	C	T
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	PWD/PhJ
rs50672238					SNP	C	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
ss60244869	NES15748710	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr16:85850599 () rs orientation: forward

Symbol	Name	Function Class
1700007H22Rik	RIKEN cDNA 1700007H22 gene	within coordinates