rs107667660 SNP Detail

Summary

• ID
  rs107667660
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr16:77641358 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGACTGTTTA GATCATTAAC
  CTGATCCCGA TTTAATTTTG TTACCCTCTA TCTGTCTAGA AATTTGTCTA TTTCATCCAG
  GTTTTGAGTT TTGTTGAGTA TAGCCTTTTG TAGAAGGATC TGATGGTGTT TTGGATTTCT
  TCAGGATCTG TTGTTATGTC TCCCTTTTCA TTTCTGATTT TGTTCATTAG AATGCTGTCC
  C
  TGTGCCCTCT AGTGAGTCTG ACTAAGGGTT TATCTATCTT GATTTTCTCA AAGAACCAGA
  TCCTTGTTTG GTTGATTCTT TGAATAGTTC TTCTTGTTTC CACGTGGTTG ATTTCACCAC
  TGAGTTTGAT TATTTCCTGC AGTCTACTGC TCTTGGATGA TTTTGCTTCC TTTTGTTTAA
  GAGCTTTTAG GTGTGTTGTC                                            
  
  C = C
  

  
  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
ss148395711	ENSMUSSNP6591265	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ
rs107667660					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr16:77641358 () rs orientation: forward

Symbol	Name	Function Class
Gm17333	predicted gene, 17333	1917 bp upstream