View genomic variant #0000023482

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.19377671_19377672insGCCACCTTTGGAAGAGCTGGGCTACCACATCTACTC
Published as -
GERP -
Segregation -
DB-ID PDHA1_000020
MSCV MSCV_0023482
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 0000023482 ./. - - c.1073_1074insGCCACCTTTGGAAGAGCTGGGCTACCACATCTACTC p.(Pro359_Ser370dup) - - - -
PDHA1 00000245 NM_001173454.1 0000023482 ./. - - c.1187_1188insGCCACCTTTGGAAGAGCTGGGCTACCACATCTACTC p.(Pro397_Ser408dup) - - - -
PDHA1 00000246 NM_001173455.1 0000023482 ./. - - c.1094_1095insGCCACCTTTGGAAGAGCTGGGCTACCACATCTACTC p.(Pro366_Ser377dup) - - - -
PDHA1 00000248 NM_001173456.1 0000023482 ./. - - c.980_981insGCCACCTTTGGAAGAGCTGGGCTACCACATCTACTC p.(Pro328_Ser339dup) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV002263537;
Chromosome X:19377670..19377670
ClinVar Allele ID 1687716
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000023.10:g.19377670G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 2147189180
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000011636;
Chromosome X:19377671..19377672
ClinVar Allele ID 25928
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.19377672 19377707dup
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA121224|OMIM:300502.0019
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 606231191
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