View genomic variant #0000023485

Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377737_19377738insCAAT
Published as -
GERP -
Segregation -
DB-ID PDHA1_000022
MSCV MSCV_0023485
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 0000023485 ./. - - c.1139_1140insCAAT p.(Trp383Serfs*6) - - - -
PDHA1 00000245 NM_001173454.1 0000023485 ./. - - c.1253_1254insCAAT p.(Trp421Serfs*6) - - - -
PDHA1 00000246 NM_001173455.1 0000023485 ./. - - c.1160_1161insCAAT p.(Trp390Serfs*6) - - - -
PDHA1 00000248 NM_001173456.1 0000023485 ./. - - c.1046_1047insCAAT p.(Trp352Serfs*6) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000011627; RCV000199126; RCV000624104; RCV001753411;
Chromosome X:19377737..19377738
ClinVar Allele ID 25919
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:C3661900|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|Pyruvate dehydrogenase complex deficiency|Pyruvate dehydrogenase E1-alpha deficiency
HGVS variant names NC 000023.10:g.19377740 19377743dup
ClinVar review status reviewed by expert panel
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA121215|OMIM:300502.0010
Gene symbol:Gene id. PDHA1:5160
Molecular consequence SO:0001589|frameshift variant
Allele origin
dbSNP ID 606231189
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