View genomic variant #0000023487

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.19377758_19377761del
Published as -
GERP -
Segregation -
DB-ID PDHA1_000024
MSCV MSCV_0023487
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 0000023487 ./. - - c.1160_1163del p.(Ser390Lysfs*33) - - - -
PDHA1 00000245 NM_001173454.1 0000023487 ./. - - c.1274_1277del p.(Ser428Lysfs*33) - - - -
PDHA1 00000246 NM_001173455.1 0000023487 ./. - - c.1181_1184del p.(Ser397Lysfs*33) - - - -
PDHA1 00000248 NM_001173456.1 0000023487 ./. - - c.1067_1070del p.(Ser359Lysfs*33) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000200467; RCV001079335; RCV002363013;
Chromosome X:19377757..19377757
Allele frequencies from ESP 0.00009
Allele frequencies from ExAC 0.00006
Allele frequencies from TGP 0.00053
ClinVar Allele ID 212020
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MONDO:MONDO:0010717, MedGen:C1839413, OMIM:312170, Orphanet:79243
ClinVar preferred disease name Inborn genetic diseases|not provided|Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19377757A>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA325044
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 201156613
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000011618;
Chromosome X:19377758..19377761
ClinVar Allele ID 25910
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.19377761CAGT[1]
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Microsatellite
Sequence Ontology for variant type SO:0000289
Variant clinical sources reported ClinGen:CA121203|OMIM:300502.0001
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 606231184
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