rs27372058 SNP Detail

Summary

• ID
  rs27372058
• 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
  Chr2:152535907 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GAGGTTGGAC TGGCTAGCTG
  TGTCTCGGGG ACTCTGGAGG CTGGGGCACC TGGCCTTGGT TTTGAAGTGT GGCTCGGGTG
  CTAAGGGACA CAGTTAGCAT TCCTGGGCTC CTGTGGTACT TTCCAGTGAT GGCTTCCAGC
  TCCAGCCCTC CACCTCCTGC CCGGCAGCAG CCACAGGGCT CTTTCTGGAC CGGTTTAGGC
  R
  CTTCTCCTCC CAGAATGCTC CCCGCATATC ATGTTCCTTA CTCGGAATGT AGACCCACCC
  GGGCCTGCTG CGTGACCATT CTATGCCATG TCTCCCTCCT CCACGTGCAG CCATACTAGT
  TCCTCAGAAC ATGTTTTCCA CTCTCCCTGG CCTGTGTAAC TTTAAAGAAG CCCTCTTCAG
  GCTAGGCCCC ACCACAGTCC                                            
  
  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	CAST/EiJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ
ss37561884	NES08908826	PERLEGEN	MM_PANEL2	f	SNP	G	G	A	G	G	G	G
SNP Consensus Information
SNP					Consensus Type	A/J	AKR/J	CAST/EiJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ
rs27372058					SNP	G	G	A	G	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
ss37561884	NES08908826	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:152535907 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm75645	predicted gene, 75645			1258 bp downstream
H13	histocompatibility 13			Intron
				Noncoding-Transcript-Variant
Rr567430	regulatory region 567430			1769 bp distal
Rr567431	regulatory region 567431			1870 bp distal
Rr567432	regulatory region 567432			136 bp distal
Rr567433	regulatory region 567433			546 bp distal
Rr567434	regulatory region 567434			746 bp proximal
Tssr20823	transcription start site region 20823			999 bp upstream
Tssr20824	transcription start site region 20824			1471 bp upstream
Tssr20825	transcription start site region 20825			1520 bp upstream