Full data view for gene ACO2

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A database from the MITOchondrial DYNamics variation portal "Mitodyn.org".
 
Information The variants shown are described using the NM_001098.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA 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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 16 c.1997G>C r.(?) p.(Gly666Ala) Paternal (confirmed) - likely pathogenic (recessive) g.41923335G>C g.41527331G>C - - ACO2_000047 - PubMed: Fukada 2019 - - Germline yes - - 0 - DNA SEQ-NG-I - - neurodegeneration Fukada2019 patient PubMed: Fukada 2019 2 carriers, 1 affected F no Japan japanese 05y 0 - - 1 Thomas Foulonneau
+?/. 16 c.1997G>C r.(?) p.(Gly666Ala) Unknown - likely pathogenic (recessive) g.41923335G>C g.41527331G>C - - ACO2_000047 - - - - SUMMARY record - - - 0 - - - - - - - - - - - - - - - - - - -
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