Individual #00017022

ID_report -
Reference -
Remarks -
Gender M
Consanguinity -
Country ? (unknown)
Population ?
Age/Death -
VIP 0
Data_av -
Treatment -
Panel size 1
Diseases MRX
Owner name Andreas Tzschach


Phenotypes

mental retardation, X-linked (MRX, intellectual disability (IDX)) (MRX;IDX)   Add phenotype for this disease

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     
0000015381 - - - Unknown - - - - - - Andreas Tzschach



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000016999 DNA SEQ-NG-I - - SLC9A6 1 Andreas Tzschach



Variants

1 entry on 1 page. Showing entry 1.
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     
X Unknown +/? g.135067656_135067991del g.135985497_135985832del - - SLC9A6_000013 - - - - Unknown ? - - 0 - Andreas Tzschach SLC9A6 - - - - - 1_1i NM_006359.2:c.-6_325+5del - - r.0? p.0? - - - - - - - - - - - - - - - - - - -
Legend