rs36597629 SNP Detail

Summary

• ID
  rs36597629
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  126
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr6:117457697 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATCACCATTC TTGGAATTTT
  AAGGCAGAGA GAGATCCAGG CTTCTGGAAC TGGGCCTCAT GCAGCTGTGC CAATTGTGGG
  TCATCAGGGA AGAGAAAGGC ATTGTTGTAT TGCAAGTTCG TTGTTATATG CCAACTGGGA
  CAGGGGACAT CTGGCTCTGG GCTCATCCTT CTTAATGTAG GAGTATTAAT ATAATCACTC
  R
  ATGAGAGCTT TCATCTGAGT ACTACAGAGC ATCCTAATAG TGGTTAGCCA CAGGCCTTCA
  TCATTGACAT TCTGGATGGT TACCTATGTC AGTATCTTAC CTAACATGTT TACCCATGTC
  AGTAGAGCAC AGTGGGGTTG TTAGTGACTT CCACCCCAAA ATCAAGGGAA ACCACCTTCA
  GTAAGAAAGC AGTCTACAAA                                            
  
  R = A/G
  

  
  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	CAST/EiJ	MOLF/EiJ
ss51408553	NES13706449	PERLEGEN	MM_PANEL2	f	SNP	A	G
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ
rs36597629					SNP	A	G

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss51408553	NES13706449	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:117457697 () rs orientation: forward

Symbol	Name	Function Class
Rr637326	regulatory region 637326	888 bp distal