rs107743359 SNP Detail

Summary

• ID
  rs107743359
• Variation Type
  SNP
• Alleles
  A/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
  Chr7:18339195 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCCCCTGAGT TCACACCCAA
  GATGGCACGG GGTTAGCGCC AACCAGAACG AACCTCAGCC AATAGTCAGG CAGGTTTCCT
  TTGTCCCTGT TCCTGCTGGC ACAAGACCCT CCAGGATTTT TTGGAGCAGA TGTTGCATTC
  CACTCACCAG GGATCTCAAG ATCCTGGGTG TGCTAGGGTG CCTACAGCAT GGAGAGTCCT
  M
  TAGGGACCTT GGGACCCTCT GTCGAATACA AGCCCAAGAT GGTGCTTTCT ACTTTGGACT
  TTTAACATTT GTTCAGACTA CTATAGACTA TGGGGACTTG GGAAGTTGAA ATAAATGTAC
  TTTTTATTAT GCTATGTTTA GGTATTCCCC ACCCCCCATA CACTGATATG TTTAGACAAG
  CCTATGAAGA ACAGGGAGTG                                            
  
  M = A/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	A/J
ss148453512	ENSMUSSNP1221909	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	C
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs107743359					SNP	A	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:18339195 () rs orientation: forward

Symbol	Name	Function Class
Psg23	pregnancy-specific beta-1-glycoprotein 23	1073 bp downstream
Tssr2096	transcription start site region 2096	1768 bp downstream