rs250729905 SNP Detail

Summary

• ID
  rs250729905
• Variation Type
  SNP
• Alleles
  A/G

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

Genome Location and Flanking Sequence

• Location
  Chr3:121804433 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CATCTTTCTG GCAAAGACAA GGACAGTGGG CTGGAGGGGA
  GGTCTTTTCT AAAGTTCTTG TCTCCATGAG TAGTCATAGA AACAAAAAGT GATAAGAGCT
  R
  GAAGTGAACA GGGTGGGAGA ACAGCAGTGT AGACGGAGGC CAGGGGCTCA CCTGGGCCTG
  AGCAGTAGCC TGGTTAGAGG AGACTTGACA GTTATATTC                       
  
  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
ss320907620	CHEV_3_121713702	CHEVERUD	SCREENING_POP	f	SNP	G	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs250729905					SNP	G	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:121804433 () rs orientation: forward

Symbol	Name	Function Class
Arhgap29	Rho GTPase activating protein 29	Intron
Rr584215	regulatory region 584215	1723 bp proximal