View genomic variant #0000023484

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377731G>A
Published as -
GERP -
Segregation -
DB-ID PDHA1_000008 See all 2 reported entries
MSCV MSCV_0001536
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 LOVD




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 0000023484 ./. - - c.1133G>A p.(Arg378His) - - - -
PDHA1 00000245 NM_001173454.1 0000023484 ./. - - c.1247G>A p.(Arg416His) - - - -
PDHA1 00000246 NM_001173455.1 0000023484 ./. - - c.1154G>A p.(Arg385His) - - - -
PDHA1 00000248 NM_001173456.1 0000023484 ./. - - c.1040G>A p.(Arg347His) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000011620; RCV001267918; RCV002251895;
Chromosome X:19377731..19377731
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 25912
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243|.
ClinVar preferred disease name not provided|Pyruvate dehydrogenase E1-alpha deficiency|See cases
HGVS variant names NC 000023.10:g.19377731G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA121205|OMIM:300502.0003|UniProtKB:P08559#VAR 004966
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 137853250
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000323139;
Chromosome X:19377731..19377731
ClinVar Allele ID 270013
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000023.10:g.19377731G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10605241
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 137853250
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