rs50668356 SNP Detail

Summary

• ID
  rs50668356
• Variation Type
  SNP
• Alleles
  A

• 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
  Chr2:125902448 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AATAACTGTA ATAAGGGCAT
  GCTTAAAGTA TAGACTCTCC AATAGCGTTC CAAAAATAGA GGGGGATATT TTACAGGATT
  TGTGGCTGGG TTGATTATCC TTGATAAAAT AACATAGAAA AATACTTTAA GCATTTTAAT
  AATTTCTTGT CAAATCTCTT TCACTTTTAA ACAGATATTT TAAAATAGTA ACATGTAAAT
  A
  AGTGCTTTTG GTGTTTTCAA AACCTTTTCC TATGATTCTT CTTGTTCAAA GTAGAAGAAA
  ATAAAGTACC CTCTACTTGC TGTATAATTA ACTAACGAGA GAAAATGTCC ATTTTGTTTC
  ATGTGTGCTA CCTTACAGTT GGGCATTGTT GAACCACAGC TTTCTATTCC CATCCCCCAC
  TCCTGGCCCA GTACTTAGAA                                            
  
  A = A
  

  
  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	DBA/2J
ss147494556	ENSMUSSNP2249641	ENSEMBL	ENSEMBL_Sanger	f	SNP	A
SNP Consensus Information
SNP					Consensus Type	DBA/2J
rs50668356					SNP	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:125902448 () rs orientation: forward

Symbol	Name	Function Class
Fam227b	family with sequence similarity 227, member B	Intron
Fgf7	fibroblast growth factor 7	Intron
Rr564314	regulatory region 564314	106 bp proximal