rs32703094 SNP Detail

Summary

• ID
  rs32703094
• Variation Type
  SNP
• Alleles
  A/G

• 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
  Chr4:150691390 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGCATTGGGA ACAAAATGAT
  TATTATAGGC CATTCGTGTC AACAACATTT AGACCTCCGT GTTTGCTTGC AAGCAAAAGC
  AGGAGCTAAT TTGCAAGGCT GCCTTTGTGG AGCTGCCTTT TGATCAATGA TTGCCTGTGT
  TAATGTTTCA GTGAGCTATT GATTTCTGCA GCAGCTTTTG TTCCTGAATT TATGTGCAGC
  R
  GGTCTGCTGT GCACCATGCA TGTTTGATTA AAGTGCAGTT GACTCCGTTC CCAGTGAGGC
  TGAGAGCTGC TTCACTCCCT ATTTGTAGAA CCAGAGCTTT CCCAACATGT TCTTTTGTTT
  GTACTCAAGA CCTAGCCACC CATGCAGGCA GCAATATGCT GTTTCTAATC CTCCATGTTT
  AATCCCTCAG TGGCCATGGC                                            
  
  R = A/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	A/J	AKR/J	DBA/2J	KK/HlJ	MOLF/EiJ	NZW/LacJ	PWD/PhJ
ss46716803	NES11011457	PERLEGEN	MM_PANEL2	f	SNP	A	A	A	A	G	A	G
SNP Consensus Information
SNP					Consensus Type	A/J	AKR/J	DBA/2J	KK/HlJ	MOLF/EiJ	NZW/LacJ	PWD/PhJ
rs32703094					SNP	A	A	A	A	G	A	G

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
ss46716803	NES11011457	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:150691390 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Rere	arginine glutamic acid dipeptide (RE) repeats			Intron
				Noncoding-Transcript-Variant
Rr605351	regulatory region 605351			within coordinates