rs251785174 SNP Detail

Summary

• ID
  rs251785174
• Variation Type
  SNP
• Alleles
  C/G

• 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
  Chr2:156957978 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TCTATGTAGA CCAGGTTGGC CTCTGCCCCT TGAGTGGTGG
  AACTAAAGGT GTCTGTTACC AAGTGTGGCT TGTGACATGG ATGTGAGAGA TCTGAATTCT
  S
  ATGCTTGCAC AGCGAGCCCT CTCACTACTG AGCCGTCTCT CCGGCCCACG GTGCATACAT
  TCACATTTTG ATCCTCTTGC TTCTGCATCC CAAGTACAC                       
  
  S = C/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	LG/J	SM/J
ss320584261	CHEV_2_156941794	CHEVERUD	SCREENING_POP	f	SNP	C	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs251785174					SNP	C	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:156957978 () rs orientation: forward

Symbol	Name	Function Class
Rr568435	regulatory region 568435	1098 bp distal
Rr568436	regulatory region 568436	896 bp proximal
Rr568437	regulatory region 568437	1069 bp proximal
Rr568438	regulatory region 568438	1470 bp proximal
Samhd1	SAM domain and HD domain, 1	Intron
Tssr27143	transcription start site region 27143	1732 bp upstream