Individual #00151792

ID_report 15B135
Reference PubMed: Lerat 2017,Journal: Lerat 2017
Remarks -
Gender M
Consanguinity yes
Country France
Population -
Age at death 36y (36 years)
VIP 0
Data_av -
Treatment no
Panel size 1
Diseases PHARC
Owner name Justine Lerat
Database submission license No license selected
Created by Justine Lerat


Phenotypes

polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract (PHARC) (PHARC)   Add phenotype for this disease

AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Hearing/Loss     

Protein     

Owner     
0000124160 sensory and motor neuropathy and ataxia Familial, autosomal recessive 15y PHARC 36y 15y 28y bilateral sensorineural deafness (HP 0008619), bilateral congenital cataract (HP 0000519) progressive - Justine Lerat



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000152647 DNA SEQ-NG-IT blood - ABHD12 1 Justine Lerat



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     
20 Both (homozygous) +?/. - likely pathogenic g.25303998_25304004delins[25305006_25305048;TC] - 379_385delAACTACTinsGATTCCTTATATACCATTGTAGTCTTACTGCTTTTGGTGAACACA - ABHD12_000032 - PubMed: Lerat 2017, Journal: Lerat 2017 - - Germline yes - - 0 - Justine Lerat ABHD12 - - - - 3 NM_001042472.2:c.379_385delins[GA;317-82_317-40inv] - r.(?) p.(Asn127Aspfs*23) - - - - - - - - - - - - - - - - - - -
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