rs247346693 SNP Detail

Summary

• ID
  rs247346693
• Variation Type
  SNP
• Alleles
  A/C

• 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
  Chr6:115157092 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTCTGAGCTA CTCTGCATTC
  TCTGAAAGAG AACACCTAGG CAGTTCCTAC ATCAGTCTCC TTCGAAATGG GTTACCAAGC
  ATCTCTCTGA AACACAGTGA ATAGTCTGTA AGTAGTTTAA CTGCAAAGAA AGACTGTCCT
  TGGGCACAGA CTCTGTCTGA ACAAGGCTTT GTGTATTCTG GGGATGTCAG GATCCTACCC
  M
  GTGAGGCAGG GTTTCCTCAG GCATTCATTC AGCTTCTCTA AGAAAGGAGC TTTTCAGAGT
  TGGCTTCTGG CTTGGTTCTT CTTCATTGTG TTCCTTTGTT TTGTAGTTTT AATGATAATT
  ATGCACCTGT CAAATGCTTC AGTTACTAAT ATGCTGACAC ATCCTTATTT AATCCTCATA
  CCAGTCATAT GGAATGCTCA                                            
  
  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	LG/J	SM/J
ss321915427	CHEV_6_115130149	CHEVERUD	SCREENING_POP	f	SNP	C	A
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs247346693					SNP	C	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:115157092 () rs orientation: forward

Symbol	Name	Function Class
Rr636932	regulatory region 636932	1005 bp distal
Syn2	synapsin II	Intron