rs27372031 SNP Detail

Summary

• ID
  rs27372031
• Variation Type
  SNP
• Alleles
  G/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
  Chr2:152539615 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCTACAGAGT TGAGTTCCAA
  GACAGCCAGG GCTACACAGA GAAACCCTGT CTTGAAAAAA CAAAAAAAGA AAGAAAGAAA
  GGAAAAGAAA GCAAGCCCTG GCCCCTGCCT TACTGCCCTG AATAGTGCAT CAATCTATCT
  CTTTCACACT CTCATTGAAG AGTTTCCCGG GTACCTTAAG AAGAAAGAAA AGAAAGCAGG
  K
  CTTGTACCCT CTGACAATAG CAAACTTGCT CTTTCTTAAA GAAACCTTCC CATGAGCCTG
  AGGCCAACAG CTCTCTGGTA AGAGGGCCAC TGGGAAAGAA TAAAGTCCAC ACATACTCCC
  CCCAAAAGTC CGACATTCCA CATTGCCCAA GACCATCTTA GGCAAGAACA TGCATGGGCT
  ACAGAGCAGG ACCCTGGCTG                                            
  
  K = G/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	A/J	AKR/J	CAST/EiJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ
ss37561857	NES08908797	PERLEGEN	MM_PANEL2	f	SNP	G	G	T	T	G	G	G
SNP Consensus Information
SNP					Consensus Type	A/J	AKR/J	CAST/EiJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ
rs27372031					SNP	G	G	T	T	G	G	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
ss37561857	NES08908797	PERLEGEN	MM_PANEL	f	SNP	G/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:152539615 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm75645	predicted gene, 75645			1012 bp upstream
H13	histocompatibility 13			Intron
				Noncoding-Transcript-Variant
Rr567435	regulatory region 567435			1023 bp distal
Rr567436	regulatory region 567436			522 bp distal
Rr567437	regulatory region 567437			732 bp distal