rs27971818 SNP Detail

Summary

• ID
  rs27971818
• Variation Type
  SNP
• Alleles
  A/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  125
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:70915582 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TGTGTGAGGT CCCAGGTTCA GTCTCCGGGC CCTCCAGGCA
  GGATGATGAT CTGTGTTTGT TCTGACTGAT GGGCTAGCGT TTGTTTGCTG TTGGCTGTTG
  W
  CCTTCTGCTT AAAATGCTCT TCATTTGGCT TGAAATAGTC TTGATGTCAA AATAGTCTCA
  AATTTTTATC TTTTACCCAT ACTTCCTCTA ACTGCAGCTT                      
  
  W = A/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	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	KK/HlJ	MOLF/EiJ	NZW/LacJ
ss38124948	NES09277671	PERLEGEN	MM_PANEL2	f	SNP	A	A	T	T	T	T
SNP Consensus Information
SNP					Consensus Type	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	KK/HlJ	MOLF/EiJ	NZW/LacJ
rs27971818					SNP	A	A	T	T	T	T

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
ss38124948	NES09277671	PERLEGEN	MM_PANEL	f	SNP	A/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:70915582 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dcaf17	DDB1 and CUL4 associated factor 17			Intron
				Noncoding-Transcript-Variant
Rr558667	regulatory region 558667			904 bp distal
Tssr18238	transcription start site region 18238			1058 bp downstream