rs233670152 SNP Detail

Summary

• ID
  rs233670152
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:93967524 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    ACACTGGAT TTGGGGTTCT TCTTAGAGCA
  AATTCACCTC AGTCATGGAA GCTGGGACCT GACCTAACAG CTGCCCAGGC ACAGAACCCA
  CAGAGGCCAT AGGCTCCCCA TTGACTTCTT GATATTTAGG GTGCAGCCTC GTGTTTCTGG
  Y
  CCAGTTTCTA TCGTTAAATG TTTCCTGGCG GGTTTAGGAT TCCAAAATTT GACTTTTGCC
  CCTTGTCTCT GCACAGAAGA AAACAAGTCG TGACCACGTT GGACACGACA GGGGTACACA
  CAGTGGGGTC AGCTGCTGGG AGGAACAACA                                 
  
  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	LG/J	SM/J
ss319844430	CHEV_1_95936376	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs233670152					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:93967524 () rs orientation: forward

Symbol	Name	Function Class
Pdcd1	programmed cell death 1	Intron