View genomic variant #0000026841

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.19372621G>A
Published as -
GERP -
Segregation -
DB-ID PDHA1_000042
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 0000026841 ./. - - c.523G>A p.(Ala175Thr) - - - -
PDHA1 00000245 NM_001173454.1 0000026841 ./. - - c.637G>A p.(Ala213Thr) - - - -
PDHA1 00000246 NM_001173455.1 0000026841 ./. - - c.544G>A p.(Ala182Thr) - - - -
PDHA1 00000248 NM_001173456.1 0000026841 ./. - - c.511-846G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000680062;
Chromosome X:19372621..19372621
ClinVar Allele ID 552256
Disease database name and identifier MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243
ClinVar preferred disease name Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19372621G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 1569191372
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003325175;
Chromosome X:19372621..19372621
ClinVar Allele ID 2742730
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000023.10:g.19372621G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
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