rs33579199 SNP Detail

Summary

• ID
  rs33579199
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr6:17762128 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TAATTTGTCC ACTTAATAGT
  TAGCAGTATA TGTGTTGAGG GAGGCTAAGA GTTATTTTTA CAGAGGGAAC CTTAGTGGTT
  TCAGGTTTTA CCCTGATGTC AGCTACCAAT TATACCTAAT CTCATTCCAG AGAGTTTTAC
  TTACTGAAGT AAATGCGGTA ATGCCAGTGT CCTCTTTATT GTAGAAGCAT GTCTGAAATC
  Y
  AAATAGAATT CACACACACA CACACACACA CATACACGGT ATTATTTTAA GCTTGATTTG
  AAAAGAGAAT CTTTCTAAAT ACAAGTAGCC ACCAGCTAGT ATATGGTTGT TTTTTATGTT
  TATGTGTTTA CTTTTATTTG TCTTAAAGTC ATACATTTTT TAATTCTTTA TTTAAAGGTT
  CTGTGATACT TTAATAGATA                                            
  
  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	FVB/NJ	KK/HlJ	MOLF/EiJ	NZW/LacJ	WSB/EiJ
ss47815362	NES11711452	PERLEGEN	MM_PANEL2	f	SNP	C		T	T	T	T	T	T	T	T	C	T	T
ss133022187	ENSMUSSNP6202391	ENSEMBL	ENSEMBL_Sanger	f	SNP		C
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	FVB/NJ	KK/HlJ	MOLF/EiJ	NZW/LacJ	WSB/EiJ
rs33579199					SNP	C	C	T	T	T	T	T	T	T	T	C	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
ss47815362	NES11711452	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:17762128 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm52895	predicted gene, 52895			within coordinates
Rr379001	regulatory region 379001			793 bp downstream
Rr626856	regulatory region 626856			1806 bp proximal
St7	suppression of tumorigenicity 7			Intron
				Noncoding-Transcript-Variant
Tssr55099	transcription start site region 55099			752 bp upstream