Variant #0000698166 (NC_000023.10:g.19368151C>T, PDHA1(NM_000284.3):c.214C>T)

Individual ID 00314866
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19368151C>T
DNA change (hg38) g.19350033C>T
Published as 328C>T
ISCN -
DB-ID PDHA1_000041
Variant remarks -
Reference PubMed: Zhu 2015
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDHA1 NM_000284.3 +/. - c.214C>T r.(?) p.(Arg72Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000316040 DNA SEQ;SEQ-NG - trio WES PDHA1 1 Johan den Dunnen