rs51299910 SNP Detail

Summary

• ID
  rs51299910
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:10991618 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GAACAATCCA GAGCCCTGAG
  TTAAATATAA GTCCTGTCAT CATAGGTAAT TATAAGTATT ATTCAGTCAG CTCAACCAGT
  TCGCCCTGAG CACCACTGAC ACAAATGTAT TAGGGTTAGG GGTGAAGCTC CTTGATAACA
  CCCCCTGCCT AGCATGTGCA AGACCCTGAG TTCAATCTGG AATATGGGTA ACATCATCAG
  M
  ACATGAAATG CTAAACTGGA ACAGCATCTT TGGGTCATTC TTTTGAGTGC TAGAGGCAAC
  CTTATCCTCA TTTACAGGTC TGACTTAGAT CCGTTTCTAT TGGCACTCTC AAACTGGTCC
  ACTGCAATGG CTCTCCAGTT AGGAAGAGTC AAGAATCGGG CAACAAATGG AGAACCCCAT
  TAGCATTCCC CAGATACTCC                                            
  
  M = A/C
  

  
  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	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
ss148669463	ENSMUSSNP1544172	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	C
ss324260885	CHEV_13_10940828	CHEVERUD	SCREENING_POP	f	SNP				A	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J	LG/J	SM/J
rs51299910					SNP	C	C	C	A	C