rs49067923 SNP Detail

Summary

• ID
  rs49067923
• 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
  Chr3:123601056 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGATGTAGAA CTCGGCTACT
  TCTTTAGCAC CATTTCTTCC TGTCTGTTGC CATTCTTTCC AGCAGGATGA GAAGGACTAA
  ACCTCTTAAC CTATAAGCCA TCCCCAAATA AATGTTTTCT TTTATGAGCT GCCATTGTTA
  TTATGTCTCT TCACAGCAAC AGTATACTGG CTAAGGCATA GTTTTACTAA TTTTTACTTT
  R
  GTAAGTAATA TTAGACTTTC ATTAATTGAG TCATAAAATT TTGCTATATA AGTAATGTCA
  GTGGTAAAAT TCAACTTTTC CTGTTGGCCA TTTATCTTTG GTTTATATGA TATTTTTGAG
  AAAATATAAA ATATTTATGC ATCTAAACTA TCTTTTAAGT ATGAATTTTT TATACAAAGT
  AAAAAAATGA CTCATTTTAA                                            
  
  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	A/J	DBA/2J	LG/J	SM/J
ss135773719	ENSMUSSNP3543049	ENSEMBL	ENSEMBL_Sanger	f	SNP	G	A
ss320923138	CHEV_3_123510325	CHEVERUD	SCREENING_POP	f	SNP			A	G
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	LG/J	SM/J
rs49067923					SNP	G	A	A	G