rs46643808 SNP Detail

Summary

• ID
  rs46643808
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:154264317 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      G CTGGCTGACC AGTGAGCTCC CTGGCTCAAC CCCTTCCTCC
  AGTGCTGGGT TCACATGCAC GTGTAGCCAT GCTCAGCCAT TTACATGGAT GTTGGGGGTT
  Y
  GAACTTAGTC TTGTTGCTTT CACAGTATCC CTTCTCAACC ACTGAGCAGT TCCCCTAGTC
  CCTAGGTTTT TGTTGTTGTT TTTTTTTTGG GGGGGGAGGG G                    
  
  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	129X1/SvJ	A/J	DBA/2J
ss148099161	ENSMUSSNP6697946	ENSEMBL	ENSEMBL_Sanger	f	SNP	T	C	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs46643808					SNP	T	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:154264317 () rs orientation: forward

Symbol	Name	Function Class
Megf6	multiple EGF-like-domains 6	Intron
Rr377451	regulatory region 377451	369 bp upstream
Rr606100	regulatory region 606100	1134 bp proximal