rs214444842 SNP Detail

Summary

• ID
  rs214444842
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr2:156955678 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ACAAAAAGAC TAGGCATGTG AGCCAGGCAG TGGTGGCAGG
  TGGATTTTTA TGAGTCTAAG GACAACCTGG TCTACGTAGT GAGTTCAAGG CCAGCCAAGC
  Y
  ACATGCTGAG ACAATGCATC AACAAACAAA CAAAAGACTG ATCAGGTACT GACGTTCACA
  GCAACTTGAG GCATGAGCTC CTAGAAGGTC GGCATTTGT                       
  
  Y = C/T
  

  
  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
ss320584236	CHEV_2_156939494	CHEVERUD	SCREENING_POP	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs214444842					SNP	T	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:156955678 () rs orientation: forward

Symbol	Name	Function Class
Rr568435	regulatory region 568435	1181 bp proximal
Samhd1	SAM domain and HD domain, 1	Intron
Tssr27140	transcription start site region 27140	1223 bp upstream
Tssr27141	transcription start site region 27141	894 bp upstream
Tssr27142	transcription start site region 27142	353 bp upstream
Tssr27143	transcription start site region 27143	519 bp downstream