SiMPLOD v. 0.6.2 alpha

LH3 ARG599TRP

SiMPLOD ID
  This is the unique identifier for this mutation in the SiMPLOD database. Please use this identifier when linking information described in SiMPLOD about this mutation.
SiMPLOD3-620

Isoenzyme
  Follow the links to gather information about the LH3 isoenzyme
Lysyl Hydroxylase 3 (human) - UniProt - Full Info

Nucleotide mutation
  Follow the links to explore annotated information about the significance of the PLOD3 c.1795A>T mutation
PLOD3 NM_001084.4:c.1795A>T - NCBI RefSeq
NCBI SNP: rs200275391

Mutation type
  Current information about the clinical implications of the mutation
SNP without clinical evidence

Evidence at
protein level
  Based on available structural and biochemical information, a statement about the existence of an LH enzyme variant bearing the described mutation is provided
This variant MAY EXIST at the protein level, although no experimental evidence is currently available to support its existence.

Related Entries
  A list of related LH/PLOD variants found matching the structural position of the mutation currently visualized
SiMPLOD1-47: LH1 ARG588LEU (Uncertain significance)
SiMPLOD1-48: LH1 ARG588HIS (SNP)
SiMPLOD1-327: LH1 delta586-634 (Pathogenic)
SiMPLOD1-870: LH1 ARG588CYS (SNP)
SiMPLOD1-871: LH1 ARG588GLY (SNP)
SiMPLOD2-229: LH2a ARG598HIS (Pathogenic)
SiMPLOD2-992: LH2a ARG598CYS (SNP)
SiMPLOD3-690: LH3 ARG599ARG (SNP)
SiMPLOD3-691: LH3 ARG599SER (SNP)

Last Update
  An evaluation of the possible effects/implications of the mutations on the LH3 molecular structure
2021-06-23 08:38:51

The three-dimensional visualization is currently based on the homology model of full-length, dimeric human LH3 (generated using the crystal structure of full-length human LH3 as template).

You may select a different PDB model file to visualize the mutation(s) using the drop-down menu below (page will refresh):

LH3 ARG599TRP
SiMPLOD ID This is the unique identifier for this mutation in the SiMPLOD database. Please use this identifier when linking information described in SiMPLOD about this mutation.	SiMPLOD3-620
Isoenzyme Follow the links to gather information about the LH3 isoenzyme	Lysyl Hydroxylase 3 (human) - UniProt - Full Info
Nucleotide mutation Follow the links to explore annotated information about the significance of the PLOD3 c.1795A>T mutation	PLOD3 NM_001084.4:c.1795A>T - NCBI RefSeq NCBI SNP: rs200275391
Mutation type Current information about the clinical implications of the mutation	SNP without clinical evidence
Evidence at protein level Based on available structural and biochemical information, a statement about the existence of an LH enzyme variant bearing the described mutation is provided	This variant MAY EXIST at the protein level, although no experimental evidence is currently available to support its existence.
Related Entries A list of related LH/PLOD variants found matching the structural position of the mutation currently visualized	SiMPLOD1-47: LH1 ARG588LEU (Uncertain significance) SiMPLOD1-48: LH1 ARG588HIS (SNP) SiMPLOD1-327: LH1 delta586-634 (Pathogenic) SiMPLOD1-870: LH1 ARG588CYS (SNP) SiMPLOD1-871: LH1 ARG588GLY (SNP) SiMPLOD2-229: LH2a ARG598HIS (Pathogenic) SiMPLOD2-992: LH2a ARG598CYS (SNP) SiMPLOD3-690: LH3 ARG599ARG (SNP) SiMPLOD3-691: LH3 ARG599SER (SNP)
Last Update An evaluation of the possible effects/implications of the mutations on the LH3 molecular structure	2021-06-23 08:38:51
The three-dimensional visualization is currently based on the homology model of full-length, dimeric human LH3 (generated using the crystal structure of full-length human LH3 as template). You may select a different PDB model file to visualize the mutation(s) using the drop-down menu below (page will refresh):