rs212098632 SNP Detail

Summary

• ID
  rs212098632
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:137007451 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        TAAAT GGCAGGGCTA TCTGACCCAA
  R
  TCAGCCTCCC GGAGCAACAG CTTTG                                      
  
  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	LG/J	SM/J
ss321362846	CHEV_4_136836055	CHEVERUD	SCREENING_POP	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs212098632					SNP	A	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:137007451 () rs orientation: forward

Symbol	Name	Function Class
Rr602577	regulatory region 602577	1130 bp distal
Rr602578	regulatory region 602578	393 bp distal
Tssr44110	transcription start site region 44110	938 bp upstream
Wnt4	wingless-type MMTV integration site family, member 4	Intron