rs47155958 SNP Detail

Summary

• ID
  rs47155958
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:144920436 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TGGTCTTCTG ACAGCTGCCC TCCTCCAGCC CCCAATACAC
  ATAAAATAAG TGTAAAATAA ATTTACTTTT CCAGGAAACT ATTGTCGTTT TGTACCCATG
  Y
  TCTGCCCCTT CCATACTTAT TCTCGATGTA GAAGAACACA AAGTACACAT TTAAAAGTAC
  ACATGAGCTG TTAGCGCCCT ACAGATGTTC TTCTGCTCC                       
  
  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	DBA/2J	LG/J	SM/J
ss147848325	ENSMUSSNP1136733	ENSEMBL	ENSEMBL_Sanger	f	SNP	T
ss321412775	CHEV_4_144783769	CHEVERUD	SCREENING_POP	f	SNP		C	T
SNP Consensus Information
SNP					Consensus Type	DBA/2J	LG/J	SM/J
rs47155958					SNP	T	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:144920436 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cpgi15267	CpG island 15267			458 bp proximal
Rr398672	regulatory region 398672			1051 bp upstream
Rr604318	regulatory region 604318			649 bp distal
Rr604319	regulatory region 604319			within coordinates
Rr604320	regulatory region 604320			482 bp proximal
Rr604321	regulatory region 604321			1129 bp proximal
Rr604322	regulatory region 604322			1221 bp proximal
Tssr44481	transcription start site region 44481			1087 bp downstream
Tssr44482	transcription start site region 44482			1101 bp downstream
Tssr44483	transcription start site region 44483			1133 bp downstream
Vps13d	vacuolar protein sorting 13D			Intron
				Noncoding-Transcript-Variant