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This database has been moved to the LOVD 3.0 Shared installation SDHD gene
LOVD SDHD homepage

General information
Gene name Succinate dehydrogenase, subunit D
Gene symbol SDHD
Chromosome Location 11q22.3-23
Database location http://chromium.lovd.nl/LOVD2/SDH/
Curator Dr. J.P.L. Bayley and Dr. Peter E.M. Taschner
Database reference for citations Bayley et al., 2005
PubMed references View all (unique) PubMed references in the SDHD database
Date of creation January 05, 2005
Last update March 09, 2016
Version SDHD160309
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_012337.1
Transcript refseq ID NM_003002.2
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 130
Total number of individuals with variant(s) 269
Total number of variants reported 269
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NOTE CITATION: If you benefit from the use of this database and publish findings, please cite; (Bayley JP, Devilee P, Taschner PE. BMC Med Genet. 2005 Nov 16;6:39.)

SIFT (Sorting Intolerant From Tolerant) analysis of missense variants. SIFT assumes that important amino acids will be conserved, using sequence homology to predict whether an amino acid substitution will affect protein function and potentially alter the phenotype (Ng & Henikoff. Nucleic Acids Res.(2003)31(13):3812-4

The variants included in the database were derived from the published literature or submitted directly and, where necessary, annotated to conform to current HGVS mutation nomenclature. When you notice any omissions or mistakes, please let us know (thank you).

Graphical displays and utilities
Summary tables Summary of all sequence variants in the SDHD database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the SDHD database, without patient data
Complete sequence variant listing Listing of all sequence variants in the SDHD database
Variants with no known pathogenicity Listing of all SDHD variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)
Download table Download the full sequence variant table of the SDHD database in tab-delimited text format.

Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms

Links to other resources
HGNC 10683
Entrez Gene 6392
OMIM - Gene 602690
OMIM - Disease Paragangliomas
UniProtKB (SwissProt/TrEMBL) O14521
GeneCards SDHD
GeneTests SDHD
External link #1 Orphanet
External link #2 Visitor Statistics - SDH Database

Copyright & disclaimer
Disclaimer: Inclusion of sequence variants in the SDH mutation database does not imply that there is convincing evidence for pathogenicity.