rs36659622 SNP Detail

Summary

• ID
  rs36659622
• Variation Type
  SNP
• Alleles
  C/T

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

Genome Location and Flanking Sequence

• Location
  Chr3:122070588 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ATCAGACAGT GATGAGAATA
  AGGATGAGTC TAGTGACGAA GAAGACTTGC TCAGTAACAC CAAGTCTAAG CTGTAAGTAC
  TGCCTCGGAA AGGAAACTGG GGAGGCCATG CTGAGGCGCA CAGCTGTGGC CGCAGCATGG
  CAAGTGTGCC CTTCCCTCAG CCTCCAAAGT AATGTTTATA GCATGTGTTG TAATAGTGTC
  Y
  CATTTAGTGT TTTCATGTGT GTATTGTGTA GAGGTTGCGT GCCCCTCAGG CTCATCCCCA
  CTGATGGATG CTCCTTTCCC CACCTAGCCC TCTTTCTGCT TTCCATGTCT TCCAGGGACA
  TGGGTGGCCC AGTGGGTTTA ATGCTTACGG GACTGTGGAT CAGGGGTTAT TTAGAAGCTC
  ACAAGCTTAC TGACTAGTTA                                            
  
  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	129S1/SvImJ	129X1/SvJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss51020904	NES13905130	PERLEGEN	MM_PANEL2	f	SNP	C		T	T	T	T	T	T	T	T	T	T	T	T	T	T
ss135737975	ENSMUSSNP3119777	ENSEMBL	ENSEMBL_Sanger	f	SNP		C	T						T
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
rs36659622					SNP	C	C	T	T	T	T	T	T	T	T	T	T	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
ss51020904	NES13905130	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:122070588 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dnttip2	deoxynucleotidyltransferase, terminal, interacting protein 2			Intron
				Noncoding-Transcript-Variant
Gm17494	predicted gene, 17494			within coordinates
Rr584274	regulatory region 584274			1918 bp distal
Tssr31492	transcription start site region 31492			1359 bp downstream