Individual #00080768

ID_report -
Reference -
Remarks -
Gender -
Consanguinity -
Country Germany
Population -
Age at death -
VIP 0
Data_av -
Treatment -
Panel size 1
Diseases HNPCC4
Owner name Gemeinschaftspraxis für Humangenetik Dresden
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Gemeinschaftspraxis für Humangenetik Dresden


Phenotypes

cancer, colorectal, nonpolyposis, hereditary, type 4 (HNPCC-4) (HNPCC4)   Add phenotype for this disease

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Diagnosis/Criteria     

Tumor/MSI     

Owner     
0000060794 - - - Unknown - - - - - - - Gemeinschaftspraxis für Humangenetik Dresden



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000080879 DNA SEQ - - PMS2 1 Gemeinschaftspraxis für Humangenetik Dresden



Variants

1 entry on 1 page. Showing entry 1.
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Chr     

Allele     

Effect     

Classification method     

Clinical classification     

AscendingDNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     

Gene     

IDbase Accession Number     

VariO/DNA     

VariO/Protein     

VariO/RNA     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

P-domain     

Exon_old     

Function/GVS     

Predict/AGVGD     

Predict/Grantham     

Predict/MutationTaster     

Predict/PolyPhen     

Predict/PolyPhenScore     

Predict/SIFT     

Predicted     

Type/DNA     

Conservation     

CpG     

Enzyme activity     

mRNA level     

Predict/CADD     

Predict/Splice     

Legacy protein change     

Protein level     
7 Unknown +?/. - likely pathogenic g.6045625_6045626dup g.6005994_6005995dup - - PMS2_000386 - - - - Germline - - - 0 - Gemeinschaftspraxis für Humangenetik Dresden PMS2 - - - - 2 NM_000535.6:c.60_61dup - r.(?) p.(Lys21Argfs*14) - - - - - - - - - - - - - - - - - - -
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