Sequence variations are described basically as recommended by the Ad-Hoc Nomenclature Committee of the Human Genome Variation Society (HGVS). For the most recent recommendations see the HGVS "Nomenclature for the description of sequence variants" web page. The most recent publication on the subject is by den Dunnen JT & Antonarakis SE (2000), Hum.Mut. 15: 7-12. NOTE: in all cases, unless indicated otherwise, all data of an entry are as reported by the author(s)/submitter. Path.: Variant pathogenicity, in the format Reported/Concluded; '+' indicating the variant is pathogenic, '+?' probably pathogenic, '-' no known pathogenicity, '-?' probably no pathogenicity, '?' effect unknown. Exon: Exon numbering. DNA change: Variation at DNA level. RNA change: Effect of change on RNA. = = RNA change identical to DNA change ? = unknown (=) = no significant effect expected (but no experimental proof) (0) = change expected to abolish transcription (ex4ex5del) = probably deletion of exons 4 to 5 (ex4ex5dup) = probably duplication of exons 4 to 5 +cry = activation of cryptic splice site (no sequence published) spl? = effect on splicing very likely (no experimental proof), examples; splice donor site change (nucleotides +1 to +5 affected) splice acceptor site change (nucleotides -2 to -1 affected) new intronic AG splice acceptor di-nucleotide created close to (within 15 nucleotides) of normal splice acceptor site (spl?) = might affect splicing (no experimental proof), examples; change affects first or last nucleotide of exon change creates strong splice donor or splice acceptor site in exon Protein: Predicted effect of change on protein (usually without experimental proof!) ? = unknown (0) = change expected to abolish translation ?fs = frame shift, but observed phenotype does not fit with prediction (for instance less severe phenotype (BMD) observed, more severe phenotype (DMD) expected) ?no fs = frame shift, but observed phenotype does not fit with prediction (for instance more severe phenotype (DMD) observed, less severe phenotype (BMD) expected) del = causes deletion fs = causes frame shift fs? = effect on reading frame very likely (no experimental proof) (fs?) = might affect the reading frame (no experimental proof) no fs = does not cause frame shift X = stop codon (nonsense) Custom PP2.1 score: Custom PolyPhen 2.1 score MAPP score: output score from Multivariate Analysis of Protein Polymorphism MAPP/PP2 Prior P: Prior probability of pathogenicity based on MAPP and PolyPhen-2 output Reference: Literature reference with possible link to publication in PubMed, dbSNP entry or other online resource. "Submitted:" indicates that the mutation was submitted directly to this database by the laboratory indicated. Template: Variant detected in DNA, RNA and/or Protein. DNA RNA Protein Technique: Technique used to reveal the change reported. For all methods, confirmation by sequencing (SEQ) is included. Select SEQ only when none of other techniques was used. BESS = Base Excision Sequence Scanning CMC = Chemical Mismatch Cleavage DGGE = Denaturing-Gradient Gel-Electrophoresis DHPLC = Denaturing High-Performance Liquid Chromatography DOVAM = Detection Of Virtually All Mutations (SSCA variant) DSCA = Double-Strand DNA Conformation Analysis HD = HeteroDuplex analysis IHC = Immuno-Histo-Chemistry mPCR = multiplex PCR MAPH = Multiplex Amplifiable Probe Hybridisation MLPA = Multiplex Ligation-dependent Probe Amplification PAGE = Poly-Acrylamide Gel-Electrophoresis PCR = Polymerase Chain Reaction PTT = Protein Truncation Test RT-PCR = Reverse Transcription and PCR SEQ = SEQuencing Southern = Southern Blotting SSCA = Single-Strand DNA Conformation Analysis (SSCP) Western = Western Blotting MSH2 DB-ID: Database IDentifier; When available, links to OMIM ID's are provided. Disease: Disease phenotype of the patient(s). Reference: Literature reference with possible link to publication in PubMed, dbSNP entry or other online resource. "Submitted:" indicates that the mutation was submitted directly to this database by the laboratory indicated.