View genomic variant #0000026836

Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.19368151C>T
Published as -
GERP -
Segregation -
DB-ID PDHA1_000045
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lishuang Shen




Variant on transcripts

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

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
PDHA1 00000247 NM_000284.3 0000026836 ./. - - c.214C>T p.(Arg72Cys) - - - -
PDHA1 00000245 NM_001173454.1 0000026836 ./. - - c.328C>T p.(Arg110Cys) - - - -
PDHA1 00000246 NM_001173455.1 0000026836 ./. - - c.214C>T p.(Arg72Cys) - - - -
PDHA1 00000248 NM_001173456.1 0000026836 ./. - - c.214C>T p.(Arg72Cys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000505722; RCV000624128; RCV000692713; RCV001814100; RCV001796727;
Chromosome X:19368151..19368151
ClinVar Allele ID 212004
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MONDO:MONDO:0019169, MedGen:C0034345, OMIM:PS312170, Orphanet:765, Orphanet:79243|MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243|Human Phenotype Ontology:HP:0012103, MedGen:C4023042
ClinVar preferred disease name Inborn genetic diseases|not provided|Pyruvate dehydrogenase complex deficiency|Pyruvate dehydrogenase E1-alpha deficiency|Abnormality of the mitochondrion
HGVS variant names NC 000023.10:g.19368151C>T
ClinVar review status reviewed by expert panel
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA320653|UniProtKB:P08559#VAR 004949
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 863224148
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None