rs50768629 SNP Detail

Summary

• ID
  rs50768629
• Variation Type
  SNP
• Alleles
  T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:174501406 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGACCTGTAG GTTCAATTGA
  GAGAACCTGC CTCAAAGAAT AGAGTGGAGA CTGGTCAGAG AGCACTCTTG TCATTGATTT
  TGGGCTTCCT CATGCATGAT CGCTCACCTG TATATAAGCT TGCATGCATA TATGCATGTA
  TACACTTGTA TGGACACATG TGCCCAAACA CATGTGAATA AGAATGCAGC CATACATGTA
  T
  ACTACATACA CTATTTTTAA AATACATATT AAAACATAGC CTTTAGATAT ATCTACTTAA
  ATGATAGTTT TCAGGCGGGG ATGTCTTTAA CTGAATCTTT CCTTCAATTA GTTAAACTAA
  TATGGAATGT AGTATATAAT TTTAATAAAT CTACAATAGG ACAATTGCAA TATATCCAGA
  CTTGAACAAA TATATATGAA                                            
  
  T = 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	A/J
ss146292489	ENSMUSSNP3473043	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
SNP Consensus Information
SNP					Consensus Type	A/J
rs50768629					SNP	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:174501406 () rs orientation: forward

Symbol	Name	Function Class
Fmn2	formin 2	Intron
Rr423785	regulatory region 423785	911 bp proximal
Rr423786	regulatory region 423786	984 bp proximal