rs227937135 SNP Detail

Summary

• ID
  rs227937135
• Variation Type
  SNP
• Alleles
  C/G

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

Genome Location and Flanking Sequence

• Location
  Chr2:152518911 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCAATTGTCC CACGAGAGTG
  AGGACCAGGG TTCAGATCTC ACCACTAGGG CATGTGGCAG GCCACCTGTA ATCCCAGCAC
  TTAAGGAGAC AGAGACAGGA CCCCTCAAAC CACCCGTCTA GCGGGACTAT CCAAATCGAA
  GTACTGTGGG TTCGAGTGAG AGGCAGGCCC TGTCTATATA AAAGGGGTAC ACACATGCAT
  S
  CCATAGGCAC GTGCTCCCTG TGTCATTGGG CTTGTGTAAA CTTACATTAT GCATCCCACC
  AAATAGCCAT TCCAAGGCTG TCCAGGTTTG TGCACATCTG TCCTGTAAGC CTCCTTTCCT
  GGTGGTGATT TCACAGGCTT GCTGCCCAGC TGCTGCTGGG TCACTTTGCA GTCTTGTGCT
  TCTCAGATTC ACAGTCTTTC                                            
  
  S = C/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	LG/J	SM/J
ss320563063	CHEV_2_152502727	CHEVERUD	SCREENING_POP	f	SNP	G	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs227937135					SNP	G	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:152518911 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
H13	histocompatibility 13			Intron
				Noncoding-Transcript-Variant
Rr567423	regulatory region 567423			1241 bp distal
Rr567424	regulatory region 567424			1155 bp proximal
Rr567425	regulatory region 567425			1392 bp proximal
Rr567426	regulatory region 567426			1465 bp proximal
Tssr20814	transcription start site region 20814			580 bp upstream