Individual #00033104

ID_report -
Reference -
Remarks -
Gender M
Consanguinity -
Country -
Population -
Age/Death -
VIP 0
Data_av -
Treatment -
Panel size 1
Diseases RP
Owner name Kornelia Neveling


Phenotypes

retinitis pigmentosa (RP) (RP)   Add phenotype for this disease

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     
0000026533 - - - Unknown 37y - - - - Kornelia Neveling



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000033172 DNA SEQ;SEQ-NG-S - - GUCY2D, RPGR 4 Kornelia Neveling



Variants

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Chr     

Allele     

Effect     

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     

Codon change     

IDbase Accession Number     

VariO/DNA     

VariO/Protein     

VariO/RNA     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     

P-domain     

Exon_old     

DNA/Legacy     

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     

Protein level     
17 Parent #1 -?/. g.7906519G>T g.8003201G>T - - GUCY2D_000001 predicted unknown effect on function, present at significant fraction in Exome Variant Server PubMed: Neveling 2012 - - Germline - - - 0 - Kornelia Neveling GUCY2D - - - - - 2 NM_000180.3:c.154G>T - - r.(?) p.(Ala52Ser) - - - - - - - - - - - - - - - - - - -
17 Parent #2 -?/. g.7906519G>T g.8003201G>T - - GUCY2D_000001 predicted unknown effect on function, present at significant fraction in Exome Variant Server PubMed: Neveling 2012 - - Germline - - - 0 - Kornelia Neveling GUCY2D - - - - - 2 NM_000180.3:c.154G>T - - r.(?) p.(Ala52Ser) - - - - - - - - - - - - - - - - - - -
X Parent #1 ?/. g.38147286_38147288del g.38288033_38288035del - - RPGR_000408 not segregating with disease in other family PubMed: Neveling 2012 - - Germline - - - 0 - Kornelia Neveling RPGR - - - - - 14 NM_000328.2:c.1579_1581del - - r.(?) p.(Gln527del) - - - - - - - - - - - - - - - - - - -
X Parent #1 -/. g.38182130T>C g.38322877T>C - - RPGR_000410 predicted benign PubMed: Neveling 2012 - - Germline - - - 0 - Kornelia Neveling RPGR - - - - - 3 NM_000328.2:c.223A>G - - r.(?) p.(Ile75Val) - - - - - - - - - - - - - - - - - - -
Legend