View genomic variant #0000023460

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.19371236C>T
Published as -
GERP -
Segregation -
DB-ID PDHA1_000032
MSCV MSCV_0023460
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 0000023460 ./. - - c.455C>T p.(Ser152Leu) - - - -
PDHA1 00000245 NM_001173454.1 0000023460 ./. - - c.569C>T p.(Ser190Leu) - - - -
PDHA1 00000246 NM_001173455.1 0000023460 ./. - - c.476C>T p.(Ser159Leu) - - - -
PDHA1 00000248 NM_001173456.1 0000023460 ./. - - c.455C>T p.(Ser152Leu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000578270;
Chromosome X:19371236..19371236
ClinVar Allele ID 481436
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.19371236C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA412393200
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1555933954
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