View genomic variant #0000023472

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.19375782A>C
Published as -
GERP -
Segregation -
DB-ID PDHA1_000003 See all 2 reported entries
MSCV MSCV_0001531
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00114 View details
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 0000023472 ./. - - c.844A>C p.(Met282Leu) - - - -
PDHA1 00000245 NM_001173454.1 0000023472 ./. - - c.958A>C p.(Met320Leu) - - - -
PDHA1 00000246 NM_001173455.1 0000023472 ./. - - c.865A>C p.(Met289Leu) - - - -
PDHA1 00000248 NM_001173456.1 0000023472 ./. - - c.751A>C p.(Met251Leu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000011632; RCV000127400; RCV000224670; RCV001271289; RCV002311510;
Chromosome X:19375782..19375782
Allele frequencies from ExAC 0.02070
Allele frequencies from TGP 0.04954
ClinVar Allele ID 25924
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MedGen:CN169374|MONDO:MONDO:0019169, MedGen:C0034345, OMIM:PS312170, Orphanet:765, Orphanet:79243|MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243
ClinVar preferred disease name Inborn genetic diseases|not provided|not specified|Pyruvate dehydrogenase complex deficiency|Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19375782A>C
ClinVar review status reviewed by expert panel
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA121220|OMIM:300502.0015|UniProtKB:P08559#VAR 021054
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 2229137
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