rs27330007 SNP Detail

Summary

• ID
  rs27330007
• 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
  Chr2:165667406 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TTAGCTCAGA GGGGTCTGTA
  GGCTCAGGCC GGTGCCATAC TACACATTAG CATTCTCAAT GGGGTCTCTA GGAAAGAGTT
  AGCAAAGGCC GAAGGCTGAT GAAACCCGCC TGCCCAAGTG GTCCATATGT GGGGGCAGGG
  GTCCAGGGCT GTGGCAGCTA CAGGCCAGGC CCCCTGCGGG ACAGGCAGCT GCTTAGGGAG
  Y
  TGAATCTGCT CGTAGGGACA ACAGACCCAG GATGAGCTAC TACTGAGTAG TCTAAAGAAA
  AGGACGGTCT TGGGGCCAGG GAAATGGTCC AGCGGGTAAG GCACCAGCCA TGAACTTGAT
  GGCCTGCGTT CAGTCCCCTG GAACACACAC GGAAGAAGCA GAGTCCTGAC CTCTGTAAAC
  TGTCTTCTGA CCTTCATATG                                            
  
  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	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
ss37513147	NES08876292	PERLEGEN	MM_PANEL2	f	SNP	T	T	T	T	T	T	T	T	T	C	T	T	T	C	T
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	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
rs27330007					SNP	T	T	T	T	T	T	T	T	T	C	T	T	T	C	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
ss37513147	NES08876292	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:165667406 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rr570021	regulatory region 570021			413 bp proximal
Rr570022	regulatory region 570022			628 bp proximal
Zmynd8	zinc finger, MYND-type containing 8			Intron
				Noncoding-Transcript-Variant