rs51077772 SNP Detail

Summary

• ID
  rs51077772
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr13:118895876 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        CAGAA CAAAGCTGAC TCAATCAAAC
  R
  AGAACAATTT CCCCCTATAG ACTGG                                      
  
  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	BTBR T<+> Itpr3/J	C3H/HeJ	LG/J	MOLF/EiJ	PWD/PhJ	SM/J
ss62066672	NES17155344	PERLEGEN	MM_PANEL2	f	SNP	G	G		G	A
ss324552165	CHEV_13_119548147	CHEVERUD	SCREENING_POP	f	SNP			A			G
SNP Consensus Information
SNP					Consensus Type	BTBR T<+> Itpr3/J	C3H/HeJ	LG/J	MOLF/EiJ	PWD/PhJ	SM/J
rs51077772					SNP	G	G	A	G	A	G

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
ss62066672	NES17155344	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr13:118895876 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Fgf10	fibroblast growth factor 10			Intron
				Noncoding-Transcript-Variant
Rr366762	regulatory region 366762			within coordinates