rs51557502 SNP Detail

Summary

• ID
  rs51557502
• Variation Type
  SNP
• Alleles
  C/G

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

Genome Location and Flanking Sequence

• Location
  Chr10:42404728 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGAGTGAGTT CTCTTTTTAC
  ACTGGAGGTA ATCAAATGAG GCTTGGCAGA CGTGCCTTTA CCCCCTGATC CATCTTGCCA
  GCCCATAACT ACGCCTGCTC TCTTTTGAAA GTTGAAAGCT GCCCAGACTA GCATCCAACT
  CACCTTGTAG CCCAGCCAGG TTTGTCTTTC AGCTCCCGTG CCATTGTACC GTATGTGCAG
  S
  ATTTCATTCT CCTTCCTGCC CTCAGTGTGA GCAACCCACG GCTCTCCGGT GCTGCTTATC
  ACTCTTAGCC GTGTTGGTCG CGTAGGGAGT GAGTGGATCA CTGGGCTTTT GGTGTCCATT
  TGGTGGCCAG TGTTGCTGCT GACCTTTTTT TCATTTACTC CTTGAGTCTG TGCTCTTTGG
  AGAAAAGTGG ACTGAGATAT                                            
  
  S = C/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	CAST/EiJ	MOLF/EiJ	PWD/PhJ	WSB/EiJ
ss61273595	NES16777576	PERLEGEN	MM_PANEL2	f	SNP	C	G	G	C
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ	PWD/PhJ	WSB/EiJ
rs51557502					SNP	C	G	G	C

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
ss61273595	NES16777576	PERLEGEN	MM_PANEL	f	SNP	C/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:42404728 () rs orientation: forward

Symbol	Name	Function Class
Snx3	sorting nexin 3	Intron