View genomic variant #0000023462

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.19371272A>G
Published as -
GERP -
Segregation -
DB-ID PDHA1_000034
MSCV MSCV_0023462
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 0000023462 ./. - - c.491A>G p.(Asn164Ser) - - - -
PDHA1 00000245 NM_001173454.1 0000023462 ./. - - c.605A>G p.(Asn202Ser) - - - -
PDHA1 00000246 NM_001173455.1 0000023462 ./. - - c.512A>G p.(Asn171Ser) - - - -
PDHA1 00000248 NM_001173456.1 0000023462 ./. - - c.491A>G p.(Asn164Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000578359; RCV001091316; RCV001824834;
Chromosome X:19371272..19371272
ClinVar Allele ID 481437
Disease database name and identifier MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243|MedGen:C3661900|MONDO:MONDO:0019169, MedGen:C0034345, OMIM:PS312170, Orphanet:765, Orphanet:79243
ClinVar preferred disease name Pyruvate dehydrogenase E1-alpha deficiency|not provided|Pyruvate dehydrogenase complex deficiency
HGVS variant names NC 000023.10:g.19371272A>G
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:CA412393370
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1555933963
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